| geneid | 130132 |
|---|---|
| ensemblid | ENSG00000162944.11 |
| hgncid | 26402 |
| symbol | RFTN2 |
| name | raftlin family member 2 |
| refseq_nuc | NM_144629.3 |
| refseq_prot | NP_653230.2 |
| ensembl_nuc | ENST00000295049.9 |
| ensembl_prot | ENSP00000295049.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 197568224 |
| end | 197675587 |
| strand | - |
| ver | v1.2 |
| region | chr2:197568224-197675587 |
| region5000 | chr2:197563224-197680587 |
| regionname0 | RFTN2_chr2_197568224_197675587 |
| regionname5000 | RFTN2_chr2_197563224_197680587 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 501 | 307 | 80 | 60 | 136 | 9 | 20 | 112 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0002 | 0/0 | 501 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0003 | 0/0 | 501 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0004 | 0/0 | 501 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0005 | 0/0 | 501 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1506 | 200 | 69 | 33 | 80 | 6 | 11 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| c0002 | 1/0 | 1506 | 104 | 10 | 25 | 56 | 3 | 9 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| c0003 | 0/0 | 1506 | 2 | 0 | 2 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| c0004 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| c0005 | 0/0 | 1506 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| c0006 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| c0007 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| c0008 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| c0009 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3914 | 71 | 0 | 25 | 38 | 3 | 5 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0002 | 0/0 | 3916 | 70 | 8 | 24 | 26 | 4 | 8 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0003 | 0/1 | 3915 | 59 | 18 | 10 | 28 | 2 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0004 | 1/0 | 3914 | 26 | 10 | 0 | 13 | 0 | 2 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0005 | 0/0 | 3916 | 17 | 0 | 0 | 17 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0006 | 0/0 | 3916 | 11 | 6 | 1 | 2 | 1 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0007 | 0/0 | 3917 | 7 | 2 | 1 | 3 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0008 | 0/0 | 3916 | 5 | 5 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0009 | 0/0 | 3915 | 4 | 4 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0010 | 0/0 | 3915 | 4 | 4 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0011 | 0/0 | 3915 | 4 | 4 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0012 | 0/0 | 3914 | 4 | 4 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0013 | 0/0 | 3914 | 3 | 3 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0014 | 0/0 | 3915 | 2 | 0 | 0 | 2 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0015 | 0/0 | 3916 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0016 | 0/0 | 3917 | 2 | 0 | 0 | 2 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0017 | 0/0 | 3916 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0018 | 0/0 | 3916 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0019 | 0/0 | 3912 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0020 | 0/0 | 3915 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0021 | 0/0 | 3916 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0022 | 0/0 | 3916 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0023 | 0/0 | 3916 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0024 | 0/0 | 3916 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0025 | 0/0 | 3914 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0026 | 0/0 | 3914 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0027 | 0/0 | 3915 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0028 | 0/0 | 3915 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0029 | 0/0 | 3915 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0030 | 0/0 | 3915 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0031 | 0/0 | 3915 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0032 | 0/0 | 3914 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0033 | 0/0 | 3914 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0034 | 0/0 | 3915 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0035 | 0/0 | 3915 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| t0036 | 0/0 | 3914 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1506 | 200 | 69 | 33 | 80 | 6 | 11 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0002 | 1/0 | 1506 | 104 | 10 | 25 | 56 | 3 | 9 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0006 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0007 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0009 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0002c0003 | 0/0 | 1506 | 2 | 0 | 2 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0003c0004 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0004c0005 | 0/0 | 1506 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0005c0008 | 0/0 | 1506 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5419 | 3 | 0 | 0 | 3 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0002 | 0/0 | 5421 | 62 | 7 | 21 | 22 | 4 | 8 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0003 | 0/1 | 5420 | 57 | 18 | 10 | 26 | 2 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0004 | 0/0 | 5419 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0005 | 0/0 | 5421 | 17 | 0 | 0 | 17 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0006 | 0/0 | 5421 | 9 | 6 | 0 | 2 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0007 | 0/0 | 5422 | 6 | 2 | 1 | 2 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0008 | 0/0 | 5421 | 5 | 5 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0009 | 0/0 | 5420 | 4 | 4 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0010 | 0/0 | 5420 | 4 | 4 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0011 | 0/0 | 5420 | 4 | 4 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0012 | 0/0 | 5419 | 4 | 4 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0013 | 0/0 | 5419 | 3 | 3 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0014 | 0/0 | 5420 | 2 | 0 | 0 | 2 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0015 | 0/0 | 5421 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0016 | 0/0 | 5422 | 2 | 0 | 0 | 2 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0017 | 0/0 | 5421 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0018 | 0/0 | 5421 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0019 | 0/0 | 5417 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0020 | 0/0 | 5420 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0021 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0022 | 0/0 | 5421 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0023 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0024 | 0/0 | 5421 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0025 | 0/0 | 5419 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0026 | 0/0 | 5419 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0028 | 0/0 | 5420 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0029 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0001t0031 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0002t0001 | 0/0 | 5419 | 65 | 0 | 22 | 35 | 3 | 5 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0002t0002 | 0/0 | 5421 | 5 | 0 | 1 | 4 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0002t0003 | 0/0 | 5420 | 2 | 0 | 0 | 2 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0002t0004 | 1/0 | 5419 | 24 | 8 | 0 | 13 | 0 | 2 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0002t0007 | 0/0 | 5422 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0002t0027 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0002t0030 | 0/0 | 5420 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0002t0032 | 0/0 | 5419 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0002t0033 | 0/0 | 5419 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0002t0034 | 0/0 | 5420 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0002t0035 | 0/0 | 5420 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0002t0036 | 0/0 | 5419 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0006t0006 | 0/0 | 5421 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0007t0002 | 0/0 | 5421 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0001c0009t0002 | 0/0 | 5421 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0002c0003t0001 | 0/0 | 5419 | 2 | 0 | 2 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0003c0004t0002 | 0/0 | 5421 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0004c0005t0006 | 0/0 | 5421 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| a0005c0008t0001 | 0/0 | 5419 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | copy fasta | chr2 | 197563224 | 197680587 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0007g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0007g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0008g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0010g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0010g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0010g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0012g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0012g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0013g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0013g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0014g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0014g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0015g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0015g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0016g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0016g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0017g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0017g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0018g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0019g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0020g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0021g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0022g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0023g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0024g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0025g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0026g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0028g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0029g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0001t0031g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0027g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0030g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0032g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0033g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0034g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0035g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0002t0036g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0006t0006g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0007t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0001c0009t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0002c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0002c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0003c0004t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0004c0005t0006g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| a0005c0008t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | GBR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0048 | EUR | GBR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0214 | EUR | FIN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0031 | EUR | FIN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00558 | hp1 | a0001 | c0001 | t0020 | g0135 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00621 | hp2 | a0001 | c0001 | t0007 | g0073 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00639 | hp1 | a0003 | c0004 | t0002 | g0131 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0273 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0269 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CHS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0256 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0265 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01106 | hp1 | a0001 | c0001 | t0028 | g0167 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01106 | hp2 | a0002 | c0003 | t0001 | g0227 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01168 | hp1 | a0001 | c0002 | t0033 | g0231 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0098 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01175 | hp2 | a0001 | c0006 | t0006 | g0175 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0266 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01255 | hp2 | a0005 | c0008 | t0001 | g0205 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0150 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0264 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0257 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0215 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01433 | hp1 | a0001 | c0009 | t0002 | g0309 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0254 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0055 | EUR | IBS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0050 | EUR | IBS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01516 | hp1 | a0004 | c0005 | t0006 | g0159 | EUR | IBS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0245 | EUR | IBS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0244 | EUR | IBS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01891 | hp1 | a0001 | c0001 | t0017 | g0146 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0296 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0268 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0294 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0270 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0267 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02004 | hp1 | a0001 | c0002 | t0032 | g0271 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02015 | hp2 | a0001 | c0001 | t0025 | g0308 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0285 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0130 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0258 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | CDX | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | CDX | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0209 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0239 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PEL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02451 | hp1 | a0001 | c0001 | t0029 | g0207 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02451 | hp2 | a0001 | c0001 | t0017 | g0147 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0138 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02615 | hp1 | a0001 | c0001 | t0012 | g0142 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02615 | hp2 | a0001 | c0001 | t0031 | g0058 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0053 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0210 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0182 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0263 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02698 | hp2 | a0001 | c0001 | t0018 | g0300 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0066 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02717 | hp2 | a0001 | c0001 | t0015 | g0047 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0206 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02723 | hp2 | a0001 | c0001 | t0012 | g0163 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02738 | hp1 | a0001 | c0002 | t0004 | g0253 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02809 | hp1 | a0001 | c0001 | t0023 | g0102 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02809 | hp2 | a0001 | c0002 | t0027 | g0012 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02818 | hp1 | a0001 | c0001 | t0012 | g0191 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02818 | hp2 | a0001 | c0001 | t0013 | g0072 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0154 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0288 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0144 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02965 | hp2 | a0001 | c0002 | t0004 | g0289 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02970 | hp1 | a0001 | c0001 | t0021 | g0037 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0141 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0054 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0061 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0062 | AFR | GWD | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03098 | hp2 | a0001 | c0002 | t0030 | g0013 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03139 | hp2 | a0001 | c0001 | t0015 | g0155 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03195 | hp2 | a0001 | c0001 | t0011 | g0060 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03225 | hp1 | a0001 | c0001 | t0026 | g0006 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0177 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03491 | hp2 | a0001 | c0002 | t0004 | g0283 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0084 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03516 | hp2 | a0001 | c0001 | t0019 | g0036 | AFR | ESN | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | MSL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03654 | hp2 | a0001 | c0002 | t0035 | g0282 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0262 | SAS | PJL | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | BEB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0290 | SAS | BEB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0139 | SAS | STU | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | STU | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG04199 | hp1 | a0001 | c0002 | t0034 | g0274 | SAS | STU | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0158 | SAS | STU | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | STU | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0211 | SAS | STU | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0284 | AFR | YRI | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0063 | AFR | YRI | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18940 | hp1 | a0001 | c0002 | t0004 | g0259 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18940 | hp2 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18944 | hp2 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18947 | hp1 | a0001 | c0002 | t0004 | g0238 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18949 | hp1 | a0001 | c0001 | t0007 | g0101 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18950 | hp1 | a0001 | c0002 | t0007 | g0232 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18957 | hp2 | a0001 | c0001 | t0014 | g0014 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18961 | hp1 | a0001 | c0002 | t0004 | g0306 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18962 | hp1 | a0001 | c0002 | t0036 | g0201 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18968 | hp1 | a0001 | c0002 | t0004 | g0292 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0291 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18973 | hp1 | a0001 | c0002 | t0004 | g0275 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18977 | hp1 | a0001 | c0002 | t0004 | g0225 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18980 | hp1 | a0001 | c0001 | t0014 | g0019 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0106 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18985 | hp2 | a0001 | c0001 | t0006 | g0170 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0136 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18997 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18997 | hp2 | a0001 | c0002 | t0004 | g0295 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19007 | hp2 | a0001 | c0002 | t0004 | g0233 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19011 | hp2 | a0001 | c0001 | t0016 | g0124 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0059 | AFR | LWK | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0082 | AFR | LWK | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0107 | AFR | LWK | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0208 | AFR | LWK | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19054 | hp1 | a0001 | c0002 | t0004 | g0224 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19054 | hp2 | a0001 | c0001 | t0016 | g0126 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19055 | hp1 | a0001 | c0002 | t0003 | g0200 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19055 | hp2 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19062 | hp2 | a0001 | c0002 | t0004 | g0234 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19066 | hp2 | a0001 | c0001 | t0022 | g0091 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19075 | hp2 | a0001 | c0002 | t0004 | g0260 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19077 | hp1 | a0001 | c0001 | t0024 | g0115 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19077 | hp2 | a0001 | c0002 | t0004 | g0226 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0261 | EAS | JPT | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0188 | AFR | YRI | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0052 | AFR | YRI | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0156 | AFR | ASW | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ASW | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0230 | AMR | CLM | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0051 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0064 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0190 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | USA | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | USA | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0281 | AFR | USA | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| NA20300 | hp2 | a0001 | c0007 | t0002 | g0086 | AFR | USA | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0169 | REF | REF | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0004 | g0065 | REF | REF | RFTN2_chr2_197563224_197680587 | RFTN2 | chr2 | 197563224 | 197680587 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:197572047
|
A | C | 1 | a0004 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.1467T>G | p.Phe489Leu | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1596/5419 | 1467/1506 | 489/501 | chr2 | 197572047 | ||
| chr2:197617850
|
T | G | 1 | a0002 | 2 | HG00735.hp1 HG01106.hp2 |
missense_variant | MODERATE | c.1000A>C | p.Ser334Arg | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/9 | 1129/5419 | 1000/1506 | 334/501 | chr2 | 197617850 | ||
| chr2:197633842
|
A | C | 1 | a0003 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.594T>G | p.Asn198Lys | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/9 | 723/5419 | 594/1506 | 198/501 | chr2 | 197633842 | ||
| chr2:197646565
|
G | A | 1 | a0005 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.241C>T | p.Pro81Ser | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/9 | 370/5419 | 241/1506 | 81/501 | chr2 | 197646565 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:197572071
|
G | A | 1 | a0001c0006 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.1443C>T | p.Leu481Leu | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1572/5419 | 1443/1506 | 481/501 | chr2 | 197572071 | ||
| chr2:197596024
|
T | G | 1 | a0001c0007 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.1200A>C | p.Pro400Pro | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/9 | 1329/5419 | 1200/1506 | 400/501 | chr2 | 197596024 | ||
| chr2:197644227
|
G | A | 6 | a0001c0001a0001c0006a0001c0007others(3): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
synonymous_variant | LOW | c.369C>T | p.Leu123Leu | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/9 | 498/5419 | 369/1506 | 123/501 | chr2 | 197644227 | ||
| chr2:197675450
|
G | A | 1 | a0001c0009 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.9C>T | p.Cys3Cys | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/9 | 138/5419 | 9/1506 | 3/501 | chr2 | 197675450 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:197568381
|
A | G | 4 | a0001c0001t0005a0001c0001t0016a0001c0001t0020others(1): Show | 21 | HG00558.hp1 HG02083.hp2 HG02523.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3627T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 3627 | chr2 | 197568381 | |||||
| chr2:197568456
|
A | G | 1 | a0001c0001t0023 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3552T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 3552 | chr2 | 197568456 | |||||
| chr2:197568532
|
T | C | 1 | a0001c0001t0029 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3476A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 3476 | chr2 | 197568532 | |||||
| chr2:197568690
|
C | T | 1 | a0001c0001t0022 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3318G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 3318 | chr2 | 197568690 | |||||
| chr2:197568961
|
TCTC | T | 2 | a0001c0001t0013a0001c0001t0019 | 4 | HG02818.hp2 HG02976.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3044_*3046delGAG | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 3044 | chr2 | 197568961 | |||||
| chr2:197568973
|
G | A | 1 | a0001c0001t0025 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3035C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 3035 | chr2 | 197568973 | |||||
| chr2:197569154
|
G | T | 1 | a0001c0001t0025 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2854C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2854 | chr2 | 197569154 | |||||
| chr2:197569595
|
G | A | 23 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(20): Show | 119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*2413C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2413 | chr2 | 197569595 | |||||
| chr2:197569676
|
C | T | 1 | a0001c0001t0028 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2332G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2332 | chr2 | 197569676 | |||||
| chr2:197569685
|
G | A | 1 | a0001c0002t0033 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2323C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2323 | chr2 | 197569685 | |||||
| chr2:197569788
|
C | T | 3 | a0001c0001t0015a0001c0002t0027a0001c0002t0030 | 4 | HG02717.hp2 HG02809.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2220G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2220 | chr2 | 197569788 | |||||
| chr2:197569890
|
C | T | 1 | a0001c0002t0032 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2118G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2118 | chr2 | 197569890 | |||||
| chr2:197569919
|
G | T | 1 | a0001c0001t0021 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2089C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2089 | chr2 | 197569919 | |||||
| chr2:197569929
|
C | CA | 24 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(21): Show | 170 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*2078dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2078 | chr2 | 197569929 | |||||
| chr2:197569929
|
C | CAA | 9 | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(6): Show | 30 | HG00621.hp2 HG01175.hp1 HG01175.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2077_*2078dupTT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 2078 | chr2 | 197569929 | |||||
| chr2:197570363
|
T | C | 1 | a0001c0001t0024 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1645A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1645 | chr2 | 197570363 | |||||
| chr2:197570386
|
C | A | 3 | a0001c0001t0008a0001c0001t0011a0001c0001t0017 | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1622G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1622 | chr2 | 197570386 | |||||
| chr2:197570556
|
A | G | 8 | a0001c0001t0001a0001c0002t0001a0001c0002t0032others(5): Show | 75 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1452T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1452 | chr2 | 197570556 | |||||
| chr2:197570667
|
T | C | 1 | a0001c0002t0036 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1341A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1341 | chr2 | 197570667 | |||||
| chr2:197570672
|
G | A | 1 | a0001c0002t0030 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1336C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1336 | chr2 | 197570672 | |||||
| chr2:197570725
|
G | A | 1 | a0001c0001t0017 | 2 | HG01891.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1283C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1283 | chr2 | 197570725 | |||||
| chr2:197570748
|
C | A | 1 | a0001c0001t0031 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1260G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 1260 | chr2 | 197570748 | |||||
| chr2:197571379
|
A | G | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(34): Show | 210 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*629T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 629 | chr2 | 197571379 | |||||
| chr2:197571585
|
A | AG | 19 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(16): Show | 112 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*422_*423insC | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 422 | chr2 | 197571585 | |||||
| chr2:197571590
|
A | T | 1 | a0001c0001t0018 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*418T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 418 | chr2 | 197571590 | |||||
| chr2:197571616
|
G | A | 1 | a0001c0001t0012 | 4 | HG02486.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*392C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 392 | chr2 | 197571616 | |||||
| chr2:197571667
|
C | T | 1 | a0001c0001t0014 | 2 | NA18957.hp2 NA18980.hp1 |
3_prime_UTR_variant | MODIFIER | c.*341G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 9/9 | 341 | chr2 | 197571667 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:197572423
|
C | T | 1 | a0001c0001t0003g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1234-143G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572423 | ||||||
| chr2:197572548
|
C | T | 4 | a0001c0001t0015g0047a0001c0001t0015g0155a0001c0002t0027g0012others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-268G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572548 | ||||||
| chr2:197572553
|
C | T | 1 | a0001c0002t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1234-273G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572553 | ||||||
| chr2:197572662
|
C | G | 195 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1234-382G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572662 | ||||||
| chr2:197572701
|
T | C | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-421A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572701 | ||||||
| chr2:197572743
|
T | C | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1234-463A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572743 | ||||||
| chr2:197572805
|
TG | T | 17 | a0001c0001t0002g0043a0001c0001t0002g0048a0001c0001t0002g0055others(14): Show | 17 | HG00099.hp2 HG00642.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1234-526delC | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572805 | ||||||
| chr2:197572860
|
A | G | 1 | a0001c0001t0012g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1234-580T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197572860 | ||||||
| chr2:197573012
|
C | T | 1 | a0001c0001t0007g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1234-732G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573012 | ||||||
| chr2:197573105
|
G | A | 51 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0011others(48): Show | 52 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1234-825C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573105 | ||||||
| chr2:197573112
|
G | T | 4 | a0001c0001t0015g0047a0001c0001t0015g0155a0001c0002t0027g0012others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-832C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573112 | ||||||
| chr2:197573114
|
G | A | 2 | a0001c0001t0006g0158a0004c0005t0006g0159 | 2 | HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1234-834C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573114 | ||||||
| chr2:197573299
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1234-1019C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573299 | ||||||
| chr2:197573393
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1234-1113G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573393 | ||||||
| chr2:197573576
|
G | A | 2 | a0001c0001t0006g0158a0004c0005t0006g0159 | 2 | HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1234-1296C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573576 | ||||||
| chr2:197573583
|
T | C | 1 | a0001c0002t0001g0229 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1234-1303A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573583 | ||||||
| chr2:197573701
|
T | C | 97 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1234-1421A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573701 | ||||||
| chr2:197573892
|
C | T | 6 | a0001c0002t0001g0212a0001c0002t0001g0213a0001c0002t0001g0239others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-1612G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197573892 | ||||||
| chr2:197574318
|
G | C | 1 | a0001c0001t0003g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1234-2038C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574318 | ||||||
| chr2:197574376
|
T | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-2096A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574376 | ||||||
| chr2:197574397
|
A | C | 1 | a0001c0001t0002g0307 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1234-2117T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574397 | ||||||
| chr2:197574536
|
AC | A | 119 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1234-2257delG | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574536 | ||||||
| chr2:197574590
|
G | T | 1 | a0001c0001t0003g0150 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1234-2310C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574590 | ||||||
| chr2:197574870
|
AAAAC | A | 202 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.1234-2594_1234-259 others(8): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574870 | ||||||
| chr2:197574999
|
G | A | 1 | a0001c0001t0009g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1234-2719C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197574999 | ||||||
| chr2:197575191
|
G | A | 1 | a0001c0002t0001g0250 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1234-2911C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575191 | ||||||
| chr2:197575380
|
G | A | 5 | a0001c0001t0008g0063a0001c0001t0011g0059a0001c0001t0011g0060others(2): Show | 5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234-3100C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575380 | ||||||
| chr2:197575647
|
C | T | 1 | a0001c0002t0001g0257 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1234-3367G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575647 | ||||||
| chr2:197575753
|
A | T | 2 | a0001c0001t0012g0142a0001c0001t0012g0190 | 2 | HG02486.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1234-3473T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575753 | ||||||
| chr2:197575753
|
AT | A | 10 | a0001c0001t0002g0043a0001c0001t0002g0055a0001c0001t0002g0056others(7): Show | 10 | HG00642.hp1 HG01070.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1234-3474delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575753 | ||||||
| chr2:197575761
|
T | A | 2 | a0001c0002t0001g0239a0001c0002t0001g0258 | 2 | HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1234-3481A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575761 | ||||||
| chr2:197575792
|
TTA | T | 4 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(1): Show | 6 | HG02559.hp2 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-3514_1234-351 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575792 | ||||||
| chr2:197575794
|
A | ATATATAT others(22): Show |
63 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0011others(60): Show | 64 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.1234-3543_1234-351 others(33): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575794 | ||||||
| chr2:197575796
|
A | G | 2 | a0001c0001t0002g0143a0001c0001t0009g0051 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1234-3516T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575796 | ||||||
| chr2:197575832
|
ATATAT | A | 119 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1234-3557_1234-355 others(9): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575832 | ||||||
| chr2:197575847
|
T | A | 3 | a0001c0001t0005g0088a0002c0003t0001g0227a0002c0003t0001g0256 | 3 | HG00735.hp1 HG01106.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1234-3567A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575847 | ||||||
| chr2:197575849
|
T | G | 4 | a0001c0002t0001g0139a0001c0002t0001g0211a0001c0002t0001g0228others(1): Show | 4 | HG01099.hp1 HG01123.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-3569A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575849 | ||||||
| chr2:197575879
|
TTATATAT others(2): Show |
T | 5 | a0001c0001t0002g0043a0001c0001t0002g0055a0001c0001t0002g0056others(2): Show | 5 | HG01243.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234-3608_1234-360 others(13): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575879 | ||||||
| chr2:197575896
|
A | AAT | 6 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0002t0001g0222others(3): Show | 6 | HG00621.hp1 HG02027.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234-3618_1234-361 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575896 | ||||||
| chr2:197575935
|
G | GCTAAGTC others(5): Show |
1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-3656_1234-365 others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575935 | ||||||
| chr2:197575936
|
G | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-3656C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575936 | ||||||
| chr2:197575993
|
G | T | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1234-3713C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197575993 | ||||||
| chr2:197576015
|
T | G | 3 | a0001c0001t0003g0001a0001c0001t0003g0027a0001c0001t0003g0028 | 4 | NA18946.hp1 NA18951.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-3735A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576015 | ||||||
| chr2:197576075
|
C | A | 1 | a0001c0001t0002g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1234-3795G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576075 | ||||||
| chr2:197576157
|
C | T | 4 | a0001c0002t0001g0139a0001c0002t0001g0211a0001c0002t0001g0228others(1): Show | 4 | HG01099.hp1 HG01123.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-3877G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576157 | ||||||
| chr2:197576295
|
T | C | 1 | a0001c0002t0004g0259 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1234-4015A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576295 | ||||||
| chr2:197576468
|
A | G | 1 | a0001c0001t0012g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1234-4188T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576468 | ||||||
| chr2:197576776
|
T | C | 1 | a0001c0002t0001g0195 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1234-4496A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576776 | ||||||
| chr2:197576887
|
C | T | 1 | a0001c0001t0018g0300 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1234-4607G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197576887 | ||||||
| chr2:197577298
|
G | A | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1234-5018C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197577298 | ||||||
| chr2:197577560
|
A | G | 1 | a0001c0002t0001g0255 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1234-5280T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197577560 | ||||||
| chr2:197577766
|
C | T | 4 | a0001c0001t0002g0048a0001c0001t0002g0301a0001c0001t0002g0302others(1): Show | 4 | HG00099.hp2 HG01123.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-5486G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197577766 | ||||||
| chr2:197578088
|
G | A | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-5808C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578088 | ||||||
| chr2:197578145
|
T | C | 1 | a0001c0001t0003g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1234-5865A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578145 | ||||||
| chr2:197578371
|
AAC | A | 120 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1234-6093_1234-609 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578371 | ||||||
| chr2:197578385
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1234-6105A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578385 | ||||||
| chr2:197578762
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-6482G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578762 | ||||||
| chr2:197578809
|
C | G | 2 | a0001c0001t0003g0057a0001c0001t0003g0071 | 2 | HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1234-6529G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578809 | ||||||
| chr2:197578932
|
C | T | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1234-6652G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578932 | ||||||
| chr2:197578999
|
C | T | 4 | a0001c0002t0001g0219a0001c0002t0001g0265a0001c0002t0001g0266others(1): Show | 4 | HG00738.hp2 HG01192.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-6719G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197578999 | ||||||
| chr2:197579055
|
T | C | 1 | a0001c0002t0004g0188 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1234-6775A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579055 | ||||||
| chr2:197579098
|
G | A | 1 | a0001c0002t0001g0222 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1234-6818C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579098 | ||||||
| chr2:197579419
|
C | T | 1 | a0001c0002t0001g0246 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1234-7139G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579419 | ||||||
| chr2:197579473
|
T | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-7193A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579473 | ||||||
| chr2:197579614
|
G | A | 1 | a0001c0002t0001g0222 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1234-7334C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579614 | ||||||
| chr2:197579646
|
T | C | 2 | a0001c0001t0002g0090a0001c0001t0022g0091 | 2 | HG00673.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1234-7366A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579646 | ||||||
| chr2:197579899
|
C | G | 120 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1234-7619G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579899 | ||||||
| chr2:197579961
|
G | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-7681C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197579961 | ||||||
| chr2:197580094
|
C | T | 2 | a0001c0001t0003g0078a0001c0001t0006g0182 | 2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1234-7814G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580094 | ||||||
| chr2:197580147
|
T | C | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1234-7867A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580147 | ||||||
| chr2:197580157
|
C | T | 6 | a0001c0001t0003g0068a0001c0001t0003g0160a0001c0001t0012g0142others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234-7877G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580157 | ||||||
| chr2:197580245
|
T | C | 1 | a0001c0002t0001g0262 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1234-7965A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580245 | ||||||
| chr2:197580450
|
C | A | 2 | a0001c0001t0003g0057a0001c0001t0003g0071 | 2 | HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1234-8170G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580450 | ||||||
| chr2:197580450
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-8170G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580450 | ||||||
| chr2:197580607
|
C | A | 4 | a0001c0001t0009g0051a0001c0001t0009g0052a0001c0001t0009g0053others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-8327G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580607 | ||||||
| chr2:197580821
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1234-8541C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580821 | ||||||
| chr2:197580877
|
T | C | 208 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(205): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.1234-8597A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580877 | ||||||
| chr2:197580878
|
G | A | 56 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0011others(53): Show | 57 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1234-8598C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580878 | ||||||
| chr2:197580984
|
C | T | 1 | a0001c0001t0021g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1234-8704G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197580984 | ||||||
| chr2:197581053
|
T | C | 306 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(303): Show | 309 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.1234-8773A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197581053 | ||||||
| chr2:197581234
|
T | C | 1 | a0001c0001t0003g0011 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1234-8954A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197581234 | ||||||
| chr2:197581584
|
C | A | 1 | a0001c0001t0002g0297 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1234-9304G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197581584 | ||||||
| chr2:197581656
|
A | AC | 6 | a0001c0001t0002g0109a0001c0001t0002g0133a0001c0001t0003g0192others(3): Show | 6 | HG00621.hp1 HG01099.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-9377dupG | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197581656 | ||||||
| chr2:197582135
|
T | C | 194 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1234-9855A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582135 | ||||||
| chr2:197582261
|
C | T | 1 | a0001c0002t0027g0012 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1234-9981G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582261 | ||||||
| chr2:197582262
|
G | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-9982C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582262 | ||||||
| chr2:197582335
|
C | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-10055G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582335 | ||||||
| chr2:197582488
|
A | C | 1 | a0001c0002t0001g0222 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1234-10208T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582488 | ||||||
| chr2:197582549
|
C | T | 12 | a0001c0002t0001g0195a0001c0002t0001g0217a0001c0002t0001g0218others(9): Show | 12 | HG00673.hp1 HG02056.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1234-10269G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582549 | ||||||
| chr2:197582653
|
T | A | 1 | a0001c0002t0004g0275 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1234-10373A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582653 | ||||||
| chr2:197582684
|
T | C | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-10404A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582684 | ||||||
| chr2:197582814
|
G | A | 2 | a0001c0001t0006g0158a0004c0005t0006g0159 | 2 | HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1234-10534C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582814 | ||||||
| chr2:197582934
|
G | A | 1 | a0001c0002t0001g0290 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1234-10654C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582934 | ||||||
| chr2:197582951
|
C | T | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-10671G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197582951 | ||||||
| chr2:197583022
|
C | A | 1 | a0001c0001t0003g0174 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1234-10742G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583022 | ||||||
| chr2:197583100
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-10820G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583100 | ||||||
| chr2:197583101
|
G | A | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1234-10821C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583101 | ||||||
| chr2:197583129
|
A | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-10849T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583129 | ||||||
| chr2:197583272
|
T | A | 1 | a0001c0001t0003g0018 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1234-10992A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583272 | ||||||
| chr2:197583614
|
G | A | 119 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1234-11334C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583614 | ||||||
| chr2:197583624
|
C | CT | 7 | a0001c0001t0002g0110a0001c0001t0002g0153a0001c0001t0005g0106others(4): Show | 7 | HG02280.hp2 HG02630.hp1 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.1234-11345dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583624 | ||||||
| chr2:197583624
|
CT | C | 11 | a0001c0001t0002g0056a0001c0001t0002g0297a0001c0001t0003g0046others(8): Show | 11 | HG01517.hp2 HG01884.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1234-11345delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583624 | ||||||
| chr2:197583643
|
T | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1234-11363A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583643 | ||||||
| chr2:197583691
|
C | T | 1 | a0001c0001t0023g0102 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1234-11411G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583691 | ||||||
| chr2:197583703
|
T | C | 5 | a0001c0001t0008g0063a0001c0001t0011g0059a0001c0001t0011g0060others(2): Show | 5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234-11423A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583703 | ||||||
| chr2:197583953
|
G | A | 2 | a0001c0001t0015g0047a0001c0001t0015g0155 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1234-11673C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583953 | ||||||
| chr2:197583973
|
C | CT | 208 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(205): Show | 211 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.1234-11694_1234-11 others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197583973 | ||||||
| chr2:197584312
|
C | T | 2 | a0001c0001t0002g0305a0001c0001t0026g0006 | 2 | HG00738.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1233+11679G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197584312 | ||||||
| chr2:197584716
|
G | A | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1233+11275C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197584716 | ||||||
| chr2:197585014
|
G | A | 2 | a0001c0001t0005g0088a0001c0001t0005g0138 | 2 | HG02523.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1233+10977C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585014 | ||||||
| chr2:197585070
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1233+10921C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585070 | ||||||
| chr2:197585133
|
G | A | 1 | a0001c0002t0001g0296 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1233+10858C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585133 | ||||||
| chr2:197585306
|
A | T | 206 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(203): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1233+10685T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585306 | ||||||
| chr2:197585354
|
C | A | 1 | a0001c0002t0004g0064 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1233+10637G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585354 | ||||||
| chr2:197585692
|
C | T | 3 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1233+10299G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585692 | ||||||
| chr2:197585738
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1233+10253G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585738 | ||||||
| chr2:197585739
|
G | A | 1 | a0001c0001t0003g0015 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1233+10252C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585739 | ||||||
| chr2:197585761
|
C | T | 1 | a0001c0002t0032g0271 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1233+10230G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197585761 | ||||||
| chr2:197586135
|
G | A | 1 | a0001c0002t0001g0241 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1233+9856C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586135 | ||||||
| chr2:197586158
|
C | T | 4 | a0001c0001t0012g0142a0001c0001t0012g0163a0001c0001t0012g0190others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+9833G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586158 | ||||||
| chr2:197586191
|
G | C | 1 | a0001c0001t0005g0187 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1233+9800C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586191 | ||||||
| chr2:197586229
|
C | T | 1 | a0001c0002t0004g0260 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1233+9762G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586229 | ||||||
| chr2:197586271
|
T | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+9720A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586271 | ||||||
| chr2:197586386
|
G | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+9605C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586386 | ||||||
| chr2:197586529
|
C | T | 1 | a0001c0001t0003g0192 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1233+9462G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586529 | ||||||
| chr2:197586534
|
C | T | 3 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0007g0098 | 3 | HG01069.hp2 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1233+9457G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586534 | ||||||
| chr2:197586818
|
G | A | 2 | a0001c0002t0001g0257a0001c0002t0033g0231 | 2 | HG01168.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1233+9173C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586818 | ||||||
| chr2:197586867
|
T | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+9124A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586867 | ||||||
| chr2:197586953
|
C | G | 1 | a0001c0002t0001g0249 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1233+9038G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197586953 | ||||||
| chr2:197587031
|
C | A | 6 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(3): Show | 8 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1233+8960G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587031 | ||||||
| chr2:197587177
|
C | A | 1 | a0001c0002t0001g0203 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1233+8814G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587177 | ||||||
| chr2:197587367
|
C | T | 3 | a0001c0001t0003g0168a0001c0001t0003g0176a0001c0001t0028g0167 | 3 | HG01070.hp2 HG01106.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1233+8624G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587367 | ||||||
| chr2:197587401
|
G | T | 1 | a0001c0001t0002g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1233+8590C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587401 | ||||||
| chr2:197587529
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+8462G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587529 | ||||||
| chr2:197587630
|
C | T | 1 | a0001c0001t0002g0279 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1233+8361G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587630 | ||||||
| chr2:197587693
|
G | A | 4 | a0001c0001t0012g0142a0001c0001t0012g0163a0001c0001t0012g0190others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+8298C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587693 | ||||||
| chr2:197587801
|
A | T | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1233+8190T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587801 | ||||||
| chr2:197587874
|
G | A | 1 | a0001c0001t0005g0088 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1233+8117C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587874 | ||||||
| chr2:197587934
|
A | G | 1 | a0001c0002t0001g0278 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1233+8057T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197587934 | ||||||
| chr2:197588113
|
T | C | 1 | a0001c0001t0005g0151 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1233+7878A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588113 | ||||||
| chr2:197588258
|
G | C | 6 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(3): Show | 8 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1233+7733C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588258 | ||||||
| chr2:197588355
|
T | A | 1 | a0001c0001t0011g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1233+7636A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588355 | ||||||
| chr2:197588394
|
T | C | 5 | a0001c0001t0008g0063a0001c0001t0011g0059a0001c0001t0011g0060others(2): Show | 5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1233+7597A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588394 | ||||||
| chr2:197588721
|
T | C | 1 | a0001c0002t0001g0258 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1233+7270A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588721 | ||||||
| chr2:197588796
|
C | G | 1 | a0001c0001t0005g0088 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1233+7195G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588796 | ||||||
| chr2:197588885
|
C | T | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1233+7106G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588885 | ||||||
| chr2:197588961
|
C | T | 114 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1233+7030G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197588961 | ||||||
| chr2:197589006
|
G | A | 5 | a0001c0001t0008g0063a0001c0001t0011g0059a0001c0001t0011g0060others(2): Show | 5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1233+6985C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589006 | ||||||
| chr2:197589012
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1233+6979T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589012 | ||||||
| chr2:197589145
|
T | C | 1 | a0001c0001t0007g0073 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1233+6846A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589145 | ||||||
| chr2:197589217
|
C | A | 5 | a0001c0001t0003g0160a0001c0001t0012g0142a0001c0001t0012g0163others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+6774G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589217 | ||||||
| chr2:197589219
|
C | CA | 29 | a0001c0001t0001g0162a0001c0001t0006g0154a0001c0001t0007g0082others(26): Show | 29 | HG00673.hp1 HG01099.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1233+6771dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | ||||||
| chr2:197589219
|
C | CAA | 44 | a0001c0001t0001g0161a0001c0001t0006g0156a0001c0001t0008g0004others(41): Show | 44 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1233+6770_1233+677 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | ||||||
| chr2:197589219
|
C | CAAA | 19 | a0001c0001t0006g0157a0001c0002t0001g0189a0001c0002t0001g0203others(16): Show | 19 | HG00642.hp2 HG00738.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1233+6769_1233+677 others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | ||||||
| chr2:197589219
|
C | CAAAA | 9 | a0001c0001t0025g0308a0001c0002t0001g0239a0001c0002t0001g0242others(6): Show | 9 | HG00733.hp2 HG01928.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.1233+6768_1233+677 others(8): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | ||||||
| chr2:197589219
|
CA | C | 34 | a0001c0001t0002g0178a0001c0001t0002g0183a0001c0001t0002g0301others(31): Show | 34 | HG01175.hp2 HG01243.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.1233+6771delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | ||||||
| chr2:197589219
|
CAA | C | 66 | a0001c0001t0002g0056a0001c0001t0002g0067a0001c0001t0002g0075others(63): Show | 67 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1233+6770_1233+677 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | ||||||
| chr2:197589219
|
CAAA | C | 69 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(66): Show | 69 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.1233+6769_1233+677 others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | ||||||
| chr2:197589219
|
CAAAA | C | 7 | a0001c0001t0002g0114a0001c0001t0002g0121a0001c0001t0002g0202others(4): Show | 7 | HG01070.hp1 HG01891.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1233+6768_1233+677 others(8): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | ||||||
| chr2:197589219
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1233+6760_1233+677 others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | ||||||
| chr2:197589219
|
CAAAAAAA others(9): Show |
C | 6 | a0001c0001t0003g0068a0001c0001t0009g0051a0001c0001t0009g0052others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233+6756_1233+677 others(20): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589219 | ||||||
| chr2:197589355
|
G | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+6636C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589355 | ||||||
| chr2:197589555
|
T | C | 1 | a0001c0001t0019g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1233+6436A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589555 | ||||||
| chr2:197589616
|
T | C | 2 | a0001c0001t0007g0084a0001c0001t0023g0102 | 2 | HG02809.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1233+6375A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589616 | ||||||
| chr2:197589807
|
T | C | 1 | a0001c0001t0011g0059 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1233+6184A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589807 | ||||||
| chr2:197589967
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1233+6024G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197589967 | ||||||
| chr2:197590056
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+5935G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590056 | ||||||
| chr2:197590066
|
C | T | 48 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0011others(45): Show | 49 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1233+5925G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590066 | ||||||
| chr2:197590126
|
C | A | 6 | a0001c0001t0003g0160a0001c0001t0012g0142a0001c0001t0012g0163others(3): Show | 6 | HG02015.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1233+5865G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590126 | ||||||
| chr2:197590194
|
C | T | 1 | a0001c0001t0006g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1233+5797G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590194 | ||||||
| chr2:197590195
|
G | A | 1 | a0001c0002t0001g0237 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1233+5796C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590195 | ||||||
| chr2:197590239
|
G | A | 1 | a0001c0002t0001g0216 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1233+5752C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590239 | ||||||
| chr2:197590319
|
T | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+5672A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590319 | ||||||
| chr2:197590449
|
C | T | 1 | a0001c0001t0012g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1233+5542G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590449 | ||||||
| chr2:197590575
|
T | G | 1 | a0001c0001t0002g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1233+5416A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590575 | ||||||
| chr2:197590617
|
T | C | 1 | a0001c0002t0002g0264 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1233+5374A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590617 | ||||||
| chr2:197590620
|
T | G | 1 | a0001c0001t0002g0297 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1233+5371A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590620 | ||||||
| chr2:197590634
|
G | A | 2 | a0001c0002t0027g0012a0001c0002t0030g0013 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1233+5357C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590634 | ||||||
| chr2:197590705
|
C | G | 119 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1233+5286G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590705 | ||||||
| chr2:197590725
|
C | T | 1 | a0001c0001t0002g0202 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1233+5266G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590725 | ||||||
| chr2:197590743
|
G | A | 1 | a0001c0002t0001g0216 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1233+5248C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590743 | ||||||
| chr2:197590793
|
G | T | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233+5198C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590793 | ||||||
| chr2:197590798
|
C | T | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1233+5193G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590798 | ||||||
| chr2:197590808
|
C | T | 12 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(9): Show | 12 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1233+5183G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590808 | ||||||
| chr2:197590829
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+5162G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590829 | ||||||
| chr2:197590883
|
G | A | 46 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0011others(43): Show | 47 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.1233+5108C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590883 | ||||||
| chr2:197590893
|
A | T | 1 | a0001c0001t0005g0122 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1233+5098T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590893 | ||||||
| chr2:197590921
|
A | T | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1233+5070T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590921 | ||||||
| chr2:197590970
|
G | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+5021C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590970 | ||||||
| chr2:197590997
|
TG | T | 5 | a0001c0001t0003g0160a0001c0001t0012g0142a0001c0001t0012g0163others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+4993delC | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197590997 | ||||||
| chr2:197591202
|
C | T | 1 | a0001c0002t0004g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1233+4789G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591202 | ||||||
| chr2:197591268
|
A | T | 5 | a0001c0001t0003g0160a0001c0001t0012g0142a0001c0001t0012g0163others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+4723T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591268 | ||||||
| chr2:197591340
|
T | C | 48 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0011others(45): Show | 49 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1233+4651A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591340 | ||||||
| chr2:197591410
|
C | T | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233+4581G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591410 | ||||||
| chr2:197591495
|
A | G | 2 | a0002c0003t0001g0227a0002c0003t0001g0256 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1233+4496T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591495 | ||||||
| chr2:197591528
|
G | A | 1 | a0001c0001t0005g0088 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1233+4463C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591528 | ||||||
| chr2:197591573
|
C | T | 3 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1233+4418G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591573 | ||||||
| chr2:197591578
|
C | A | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1233+4413G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591578 | ||||||
| chr2:197591586
|
C | A | 98 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1233+4405G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591586 | ||||||
| chr2:197591616
|
T | C | 7 | a0001c0001t0002g0043a0001c0001t0002g0055a0001c0001t0002g0056others(4): Show | 7 | HG01099.hp2 HG01243.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1233+4375A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591616 | ||||||
| chr2:197591658
|
G | C | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1233+4333C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591658 | ||||||
| chr2:197591702
|
G | A | 2 | a0001c0001t0002g0178a0001c0001t0007g0177 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1233+4289C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591702 | ||||||
| chr2:197591735
|
G | A | 2 | a0001c0002t0001g0244a0001c0002t0001g0245 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1233+4256C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591735 | ||||||
| chr2:197591776
|
G | A | 2 | a0001c0002t0027g0012a0001c0002t0030g0013 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1233+4215C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591776 | ||||||
| chr2:197591812
|
G | C | 3 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174 | 3 | HG00408.hp1 HG02040.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1233+4179C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591812 | ||||||
| chr2:197591825
|
C | T | 1 | a0001c0001t0003g0020 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1233+4166G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591825 | ||||||
| chr2:197591909
|
C | T | 5 | a0001c0001t0003g0068a0001c0001t0009g0051a0001c0001t0009g0052others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+4082G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591909 | ||||||
| chr2:197591932
|
G | GCCTCTCC others(7): Show |
2 | a0002c0003t0001g0227a0002c0003t0001g0256 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1233+4045_1233+405 others(18): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197591932 | ||||||
| chr2:197592073
|
G | A | 1 | a0001c0002t0001g0229 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1233+3918C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197592073 | ||||||
| chr2:197592159
|
G | C | 1 | a0001c0001t0003g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1233+3832C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197592159 | ||||||
| chr2:197592203
|
T | A | 12 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(9): Show | 12 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1233+3788A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197592203 | ||||||
| chr2:197592385
|
G | A | 12 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(9): Show | 12 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1233+3606C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197592385 | ||||||
| chr2:197592495
|
G | C | 12 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(9): Show | 12 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1233+3496C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197592495 | ||||||
| chr2:197592569
|
T | G | 4 | a0001c0001t0013g0054a0001c0001t0013g0072a0001c0001t0013g0107others(1): Show | 4 | HG02818.hp2 HG02976.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+3422A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197592569 | ||||||
| chr2:197593122
|
T | C | 3 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1233+2869A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197593122 | ||||||
| chr2:197593555
|
A | AT | 48 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0011others(45): Show | 49 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1233+2435dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197593555 | ||||||
| chr2:197593655
|
G | A | 1 | a0001c0002t0001g0270 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1233+2336C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197593655 | ||||||
| chr2:197593716
|
A | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+2275T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197593716 | ||||||
| chr2:197593720
|
C | G | 12 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(9): Show | 12 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1233+2271G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197593720 | ||||||
| chr2:197593807
|
A | C | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+2184T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197593807 | ||||||
| chr2:197594015
|
C | CT | 11 | a0001c0002t0001g0217a0001c0002t0001g0244a0001c0002t0001g0252others(8): Show | 11 | HG01106.hp2 HG01517.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1233+1975dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594015 | ||||||
| chr2:197594015
|
CT | C | 202 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.1233+1975delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594015 | ||||||
| chr2:197594078
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+1913G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594078 | ||||||
| chr2:197594173
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1233+1818C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594173 | ||||||
| chr2:197594241
|
C | T | 1 | a0001c0001t0019g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1233+1750G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594241 | ||||||
| chr2:197594429
|
G | C | 4 | a0001c0001t0012g0142a0001c0001t0012g0163a0001c0001t0012g0190others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+1562C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594429 | ||||||
| chr2:197594622
|
G | A | 5 | a0001c0001t0003g0160a0001c0001t0012g0142a0001c0001t0012g0163others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+1369C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594622 | ||||||
| chr2:197594659
|
T | C | 1 | a0001c0001t0019g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1233+1332A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594659 | ||||||
| chr2:197594692
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1233+1299A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594692 | ||||||
| chr2:197594821
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+1170G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594821 | ||||||
| chr2:197594999
|
G | T | 1 | a0001c0002t0001g0290 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1233+992C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197594999 | ||||||
| chr2:197595008
|
T | C | 2 | a0001c0002t0001g0194a0001c0002t0036g0201 | 2 | NA18962.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1233+983A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197595008 | ||||||
| chr2:197595114
|
A | C | 1 | a0001c0002t0004g0283 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1233+877T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197595114 | ||||||
| chr2:197595316
|
T | G | 48 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0011others(45): Show | 49 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1233+675A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197595316 | ||||||
| chr2:197595353
|
C | A | 1 | a0001c0001t0019g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1233+638G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197595353 | ||||||
| chr2:197595618
|
A | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+373T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 8/8 | chr2 | 197595618 | ||||||
| chr2:197596215
|
T | C | 2 | a0001c0001t0003g0171a0001c0001t0006g0170 | 2 | NA18985.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1155-146A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197596215 | ||||||
| chr2:197596355
|
C | G | 3 | a0001c0001t0002g0075a0001c0001t0002g0183a0001c0001t0007g0073 | 3 | HG00621.hp2 NA18963.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1155-286G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197596355 | ||||||
| chr2:197596429
|
C | A | 1 | a0001c0001t0002g0096 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1155-360G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197596429 | ||||||
| chr2:197596887
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1155-818C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197596887 | ||||||
| chr2:197597174
|
T | C | 1 | a0001c0002t0001g0203 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1155-1105A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197597174 | ||||||
| chr2:197597217
|
A | C | 75 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0011others(72): Show | 76 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.1155-1148T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197597217 | ||||||
| chr2:197598133
|
A | C | 5 | a0001c0001t0002g0140a0001c0001t0002g0178a0001c0001t0002g0297others(2): Show | 5 | HG01884.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1155-2064T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598133 | ||||||
| chr2:197598218
|
G | C | 8 | a0001c0001t0002g0143a0001c0001t0003g0068a0001c0001t0009g0051others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1155-2149C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598218 | ||||||
| chr2:197598366
|
G | T | 199 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1155-2297C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598366 | ||||||
| chr2:197598586
|
T | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1155-2517A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598586 | ||||||
| chr2:197598781
|
G | T | 1 | a0001c0002t0001g0237 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1155-2712C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598781 | ||||||
| chr2:197598958
|
CT | C | 6 | a0001c0001t0002g0048a0001c0001t0002g0186a0001c0001t0002g0304others(3): Show | 6 | HG00099.hp1 HG00099.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1155-2890delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598958 | ||||||
| chr2:197598967
|
T | G | 29 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(26): Show | 29 | HG00621.hp2 HG00735.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.1155-2898A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598967 | ||||||
| chr2:197598998
|
C | A | 1 | a0001c0001t0003g0015 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1155-2929G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197598998 | ||||||
| chr2:197599033
|
G | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1155-2964C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197599033 | ||||||
| chr2:197599484
|
C | T | 1 | a0001c0001t0005g0130 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1155-3415G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197599484 | ||||||
| chr2:197599595
|
T | C | 1 | a0001c0002t0035g0282 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1155-3526A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197599595 | ||||||
| chr2:197599733
|
G | C | 3 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1155-3664C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197599733 | ||||||
| chr2:197599866
|
TA | T | 5 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(2): Show | 7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155-3798delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197599866 | ||||||
| chr2:197599885
|
T | A | 1 | a0001c0001t0003g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1155-3816A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197599885 | ||||||
| chr2:197600029
|
T | C | 1 | a0001c0001t0008g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1155-3960A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600029 | ||||||
| chr2:197600209
|
C | T | 5 | a0001c0001t0008g0063a0001c0001t0011g0059a0001c0001t0011g0060others(2): Show | 5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1155-4140G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600209 | ||||||
| chr2:197600552
|
C | T | 2 | a0001c0001t0003g0171a0001c0001t0006g0170 | 2 | NA18985.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1155-4483G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600552 | ||||||
| chr2:197600719
|
C | T | 1 | a0001c0001t0009g0053 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1155-4650G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600719 | ||||||
| chr2:197600833
|
T | C | 1 | a0001c0002t0001g0221 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1155-4764A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600833 | ||||||
| chr2:197600837
|
C | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1155-4768G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600837 | ||||||
| chr2:197600973
|
G | A | 9 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0002t0001g0222others(6): Show | 9 | HG00621.hp1 HG01928.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1155-4904C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197600973 | ||||||
| chr2:197601043
|
G | C | 3 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1155-4974C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601043 | ||||||
| chr2:197601116
|
T | C | 119 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1155-5047A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601116 | ||||||
| chr2:197601190
|
T | C | 4 | a0001c0002t0001g0189a0001c0002t0001g0269a0001c0002t0001g0272others(1): Show | 4 | HG00642.hp2 HG00733.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1155-5121A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601190 | ||||||
| chr2:197601307
|
A | G | 1 | a0001c0001t0011g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1155-5238T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601307 | ||||||
| chr2:197601313
|
T | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1155-5244A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601313 | ||||||
| chr2:197601400
|
T | C | 11 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1155-5331A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601400 | ||||||
| chr2:197601549
|
T | C | 200 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1155-5480A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601549 | ||||||
| chr2:197601567
|
A | C | 2 | a0001c0001t0006g0154a0001c0001t0006g0156 | 2 | HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1155-5498T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601567 | ||||||
| chr2:197601586
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1155-5517G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601586 | ||||||
| chr2:197601674
|
T | C | 1 | a0001c0001t0002g0079 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1155-5605A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601674 | ||||||
| chr2:197601738
|
C | A | 76 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0011others(73): Show | 77 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.1155-5669G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601738 | ||||||
| chr2:197601781
|
A | C | 3 | a0001c0001t0002g0128a0001c0001t0002g0166a0001c0001t0002g0186 | 3 | HG01168.hp2 HG01255.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1155-5712T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601781 | ||||||
| chr2:197601815
|
T | C | 13 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(10): Show | 13 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.1155-5746A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197601815 | ||||||
| chr2:197602040
|
T | C | 1 | a0001c0001t0029g0207 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1155-5971A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602040 | ||||||
| chr2:197602064
|
T | A | 5 | a0001c0001t0008g0063a0001c0001t0011g0059a0001c0001t0011g0060others(2): Show | 5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1155-5995A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602064 | ||||||
| chr2:197602150
|
C | T | 12 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(9): Show | 12 | HG02145.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1155-6081G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602150 | ||||||
| chr2:197602241
|
T | G | 13 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(10): Show | 13 | HG02015.hp2 HG02145.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1155-6172A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602241 | ||||||
| chr2:197602389
|
A | T | 46 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0011others(43): Show | 47 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.1155-6320T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602389 | ||||||
| chr2:197602417
|
C | T | 199 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1155-6348G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602417 | ||||||
| chr2:197602428
|
T | A | 1 | a0001c0001t0003g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1155-6359A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602428 | ||||||
| chr2:197602634
|
G | A | 1 | a0001c0002t0004g0281 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1155-6565C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602634 | ||||||
| chr2:197602952
|
T | C | 1 | a0001c0002t0001g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1155-6883A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197602952 | ||||||
| chr2:197603003
|
C | T | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | NA18946.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1155-6934G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603003 | ||||||
| chr2:197603056
|
C | T | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1155-6987G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603056 | ||||||
| chr2:197603087
|
T | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1155-7018A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603087 | ||||||
| chr2:197603109
|
ATATACCT others(5): Show |
A | 1 | a0001c0001t0003g0015 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1155-7052_1155-704 others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603109 | ||||||
| chr2:197603175
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1155-7106G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603175 | ||||||
| chr2:197603182
|
C | T | 1 | a0001c0002t0001g0223 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1155-7113G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603182 | ||||||
| chr2:197603255
|
C | T | 1 | a0001c0001t0017g0146 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1155-7186G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603255 | ||||||
| chr2:197603344
|
C | A | 1 | a0001c0001t0006g0030 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1155-7275G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603344 | ||||||
| chr2:197603360
|
G | A | 1 | a0001c0001t0006g0030 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1155-7291C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603360 | ||||||
| chr2:197603835
|
A | T | 1 | a0001c0001t0003g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1155-7766T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197603835 | ||||||
| chr2:197604027
|
G | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1155-7958C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604027 | ||||||
| chr2:197604740
|
C | CTATT | 6 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0002t0001g0216others(3): Show | 6 | HG02040.hp2 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1155-8675_1155-867 others(8): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604740 | ||||||
| chr2:197604740
|
C | CTATTTAT others(5): Show |
1 | a0001c0002t0001g0290 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1155-8683_1155-867 others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604740 | ||||||
| chr2:197604740
|
CTATTTAT others(1): Show |
C | 6 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(3): Show | 8 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1155-8679_1155-867 others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604740 | ||||||
| chr2:197604740
|
CTATTTAT others(5): Show |
C | 202 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(199): Show | 203 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1155-8683_1155-867 others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604740 | ||||||
| chr2:197604740
|
CTATTTAT others(9): Show |
C | 1 | a0001c0001t0018g0300 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1155-8687_1155-867 others(20): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604740 | ||||||
| chr2:197604770
|
ATTTATTT others(1): Show |
A | 4 | a0001c0002t0001g0219a0001c0002t0001g0265a0001c0002t0001g0266others(1): Show | 4 | HG00738.hp2 HG01192.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1155-8709_1155-870 others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604770 | ||||||
| chr2:197604778
|
T | A | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1155-8709A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604778 | ||||||
| chr2:197604795
|
C | G | 2 | a0001c0002t0001g0276a0001c0002t0001g0277 | 2 | NA19005.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1155-8726G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604795 | ||||||
| chr2:197604889
|
T | C | 1 | a0001c0001t0017g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1155-8820A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604889 | ||||||
| chr2:197604922
|
G | A | 7 | a0001c0001t0002g0193a0001c0001t0003g0011a0001c0001t0003g0171others(4): Show | 7 | HG00408.hp1 HG02040.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1155-8853C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197604922 | ||||||
| chr2:197605142
|
T | C | 1 | a0001c0001t0005g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1155-9073A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605142 | ||||||
| chr2:197605268
|
A | G | 2 | a0001c0001t0006g0154a0001c0001t0006g0156 | 2 | HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1155-9199T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605268 | ||||||
| chr2:197605326
|
T | C | 1 | a0001c0001t0002g0307 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1155-9257A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605326 | ||||||
| chr2:197605407
|
G | A | 1 | a0001c0001t0009g0053 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1155-9338C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605407 | ||||||
| chr2:197605409
|
G | A | 1 | a0001c0001t0007g0084 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1155-9340C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605409 | ||||||
| chr2:197605426
|
A | G | 2 | a0001c0002t0001g0244a0001c0002t0001g0245 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1155-9357T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605426 | ||||||
| chr2:197605427
|
G | C | 1 | a0001c0001t0009g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1155-9358C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605427 | ||||||
| chr2:197605431
|
G | A | 1 | a0001c0002t0001g0229 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1155-9362C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605431 | ||||||
| chr2:197605432
|
A | G | 2 | a0002c0003t0001g0227a0002c0003t0001g0256 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1155-9363T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605432 | ||||||
| chr2:197605451
|
A | G | 1 | a0001c0001t0002g0303 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1155-9382T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605451 | ||||||
| chr2:197605458
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1155-9389C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605458 | ||||||
| chr2:197605466
|
T | C | 1 | a0001c0001t0002g0303 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1155-9397A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605466 | ||||||
| chr2:197605822
|
C | T | 47 | a0001c0001t0002g0193a0001c0001t0003g0001a0001c0001t0003g0010others(44): Show | 48 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.1155-9753G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197605822 | ||||||
| chr2:197606172
|
T | C | 9 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(6): Show | 9 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1154+9704A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606172 | ||||||
| chr2:197606255
|
A | C | 1 | a0001c0002t0001g0195 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1154+9621T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606255 | ||||||
| chr2:197606283
|
T | A | 1 | a0001c0001t0002g0096 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1154+9593A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606283 | ||||||
| chr2:197606378
|
C | T | 6 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(3): Show | 8 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1154+9498G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606378 | ||||||
| chr2:197606666
|
G | A | 206 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(203): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1154+9210C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606666 | ||||||
| chr2:197606685
|
T | G | 1 | a0001c0001t0017g0146 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1154+9191A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606685 | ||||||
| chr2:197606689
|
C | T | 1 | a0001c0001t0014g0014 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1154+9187G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197606689 | ||||||
| chr2:197607030
|
C | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154+8846G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607030 | ||||||
| chr2:197607214
|
G | A | 1 | a0001c0002t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1154+8662C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607214 | ||||||
| chr2:197607251
|
G | T | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154+8625C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607251 | ||||||
| chr2:197607280
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154+8596G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607280 | ||||||
| chr2:197607288
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1154+8588G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607288 | ||||||
| chr2:197607354
|
T | G | 73 | a0001c0001t0002g0193a0001c0001t0003g0001a0001c0001t0003g0010others(70): Show | 74 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.1154+8522A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607354 | ||||||
| chr2:197607457
|
G | A | 8 | a0001c0001t0002g0143a0001c0001t0003g0068a0001c0001t0009g0051others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1154+8419C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607457 | ||||||
| chr2:197607475
|
T | TATA | 19 | a0001c0001t0002g0140a0001c0001t0002g0178a0001c0001t0002g0297others(16): Show | 19 | HG01175.hp2 HG01361.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.1154+8398_1154+840 others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | ||||||
| chr2:197607475
|
T | TATAATA | 50 | a0001c0001t0002g0193a0001c0001t0003g0001a0001c0001t0003g0010others(47): Show | 51 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.1154+8395_1154+840 others(10): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | ||||||
| chr2:197607475
|
T | TATAATAA others(2): Show |
9 | a0001c0001t0003g0002a0001c0001t0003g0015a0001c0001t0003g0148others(6): Show | 11 | HG01243.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1154+8392_1154+840 others(13): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | ||||||
| chr2:197607475
|
T | TATAATAA others(5): Show |
2 | a0001c0001t0003g0100a0001c0001t0008g0063 | 2 | HG00733.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1154+8389_1154+840 others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | ||||||
| chr2:197607475
|
TATA | T | 99 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1154+8398_1154+840 others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | ||||||
| chr2:197607475
|
TATAATA | T | 3 | a0001c0001t0012g0191a0001c0001t0025g0308a0001c0002t0001g0290 | 3 | HG02015.hp2 HG02818.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1154+8395_1154+840 others(10): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | ||||||
| chr2:197607475
|
TATAATAA others(2): Show |
T | 3 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0007g0098 | 3 | HG01069.hp2 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1154+8392_1154+840 others(13): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607475 | ||||||
| chr2:197607610
|
C | T | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154+8266G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607610 | ||||||
| chr2:197607736
|
T | C | 3 | a0001c0002t0001g0009a0001c0002t0001g0199a0001c0002t0001g0223 | 3 | HG00558.hp2 HG02165.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1154+8140A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607736 | ||||||
| chr2:197607943
|
T | C | 1 | a0001c0002t0001g0216 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1154+7933A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197607943 | ||||||
| chr2:197608162
|
A | G | 199 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1154+7714T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608162 | ||||||
| chr2:197608310
|
A | AT | 62 | a0001c0001t0002g0049a0001c0001t0002g0121a0001c0001t0002g0193others(59): Show | 65 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.1154+7565dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608310 | ||||||
| chr2:197608310
|
AT | A | 19 | a0001c0001t0002g0119a0001c0001t0003g0044a0001c0001t0003g0045others(16): Show | 19 | HG02145.hp1 HG02258.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1154+7565delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608310 | ||||||
| chr2:197608468
|
C | T | 3 | a0001c0001t0012g0142a0001c0001t0012g0190a0001c0001t0012g0191 | 3 | HG02486.hp2 HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1154+7408G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608468 | ||||||
| chr2:197608623
|
CT | C | 39 | a0001c0001t0002g0096a0001c0001t0003g0044a0001c0001t0003g0045others(36): Show | 39 | HG01175.hp2 HG01433.hp1 HG01516.hp2 others(36): Show |
intron_variant | MODIFIER | c.1154+7252delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608623 | ||||||
| chr2:197608623
|
CTT | C | 151 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(148): Show | 152 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1154+7251_1154+725 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608623 | ||||||
| chr2:197608623
|
CTTT | C | 11 | a0001c0001t0002g0055a0001c0001t0002g0097a0001c0001t0002g0119others(8): Show | 11 | HG01515.hp1 HG01516.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1154+7250_1154+725 others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608623 | ||||||
| chr2:197608787
|
C | T | 1 | a0001c0002t0004g0233 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1154+7089G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608787 | ||||||
| chr2:197608818
|
T | C | 2 | a0001c0001t0011g0060a0001c0001t0011g0061 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1154+7058A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608818 | ||||||
| chr2:197608859
|
A | G | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154+7017T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608859 | ||||||
| chr2:197608878
|
C | T | 1 | a0001c0002t0001g0249 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1154+6998G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608878 | ||||||
| chr2:197608879
|
G | A | 3 | a0001c0001t0012g0142a0001c0001t0012g0190a0001c0001t0012g0191 | 3 | HG02486.hp2 HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1154+6997C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197608879 | ||||||
| chr2:197609365
|
G | T | 5 | a0001c0001t0008g0063a0001c0001t0011g0059a0001c0001t0011g0060others(2): Show | 5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154+6511C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609365 | ||||||
| chr2:197609377
|
T | C | 6 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(3): Show | 8 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1154+6499A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609377 | ||||||
| chr2:197609403
|
A | G | 1 | a0001c0001t0023g0102 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1154+6473T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609403 | ||||||
| chr2:197609494
|
A | G | 200 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1154+6382T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609494 | ||||||
| chr2:197609511
|
C | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154+6365G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609511 | ||||||
| chr2:197609646
|
G | A | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1154+6230C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609646 | ||||||
| chr2:197609762
|
A | G | 1 | a0001c0001t0002g0097 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1154+6114T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609762 | ||||||
| chr2:197609938
|
G | A | 2 | a0001c0002t0001g0250a0001c0002t0001g0293 | 2 | NA18979.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1154+5938C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197609938 | ||||||
| chr2:197610184
|
C | T | 206 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(203): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1154+5692G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197610184 | ||||||
| chr2:197610314
|
C | T | 2 | a0001c0001t0002g0048a0001c0001t0018g0300 | 2 | HG00099.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1154+5562G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197610314 | ||||||
| chr2:197610443
|
T | G | 1 | a0001c0001t0021g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1154+5433A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197610443 | ||||||
| chr2:197610452
|
A | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154+5424T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197610452 | ||||||
| chr2:197610788
|
T | C | 1 | a0001c0001t0003g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1154+5088A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197610788 | ||||||
| chr2:197610964
|
G | A | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1154+4912C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197610964 | ||||||
| chr2:197611055
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1154+4821C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611055 | ||||||
| chr2:197611056
|
A | T | 1 | a0001c0002t0034g0274 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1154+4820T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611056 | ||||||
| chr2:197611129
|
A | G | 2 | a0001c0001t0017g0146a0001c0001t0017g0147 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1154+4747T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611129 | ||||||
| chr2:197611139
|
G | T | 2 | a0001c0002t0004g0064a0001c0002t0004g0066 | 2 | HG02486.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1154+4737C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611139 | ||||||
| chr2:197611206
|
C | G | 2 | a0001c0001t0015g0047a0001c0001t0015g0155 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1154+4670G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611206 | ||||||
| chr2:197611262
|
C | T | 1 | a0001c0001t0011g0060 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1154+4614G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611262 | ||||||
| chr2:197611414
|
T | A | 1 | a0001c0001t0003g0150 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1154+4462A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611414 | ||||||
| chr2:197611419
|
T | C | 1 | a0001c0001t0002g0143 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1154+4457A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611419 | ||||||
| chr2:197611423
|
A | T | 2 | a0001c0001t0017g0146a0001c0001t0017g0147 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1154+4453T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611423 | ||||||
| chr2:197611428
|
A | G | 18 | a0001c0001t0002g0043a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1154+4448T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611428 | ||||||
| chr2:197611480
|
C | T | 1 | a0001c0001t0003g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1154+4396G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611480 | ||||||
| chr2:197611481
|
G | A | 1 | a0001c0002t0004g0283 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1154+4395C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611481 | ||||||
| chr2:197611941
|
C | T | 5 | a0001c0001t0008g0063a0001c0001t0011g0059a0001c0001t0011g0060others(2): Show | 5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154+3935G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197611941 | ||||||
| chr2:197612488
|
T | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154+3388A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612488 | ||||||
| chr2:197612520
|
C | T | 5 | a0001c0001t0002g0079a0001c0001t0002g0090a0001c0001t0002g0097others(2): Show | 5 | HG00673.hp2 HG03942.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154+3356G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612520 | ||||||
| chr2:197612638
|
T | C | 1 | a0001c0001t0029g0207 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1154+3238A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612638 | ||||||
| chr2:197612661
|
G | A | 3 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1154+3215C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612661 | ||||||
| chr2:197612778
|
C | T | 1 | a0001c0002t0001g0262 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1154+3098G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612778 | ||||||
| chr2:197612779
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1154+3097C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612779 | ||||||
| chr2:197612882
|
G | A | 200 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1154+2994C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612882 | ||||||
| chr2:197612896
|
C | A | 116 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1154+2980G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197612896 | ||||||
| chr2:197613118
|
A | G | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1154+2758T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197613118 | ||||||
| chr2:197613596
|
G | A | 200 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1154+2280C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197613596 | ||||||
| chr2:197613869
|
G | T | 2 | a0001c0001t0009g0051a0001c0001t0009g0053 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1154+2007C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197613869 | ||||||
| chr2:197613873
|
T | C | 2 | a0001c0001t0009g0051a0001c0001t0009g0053 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1154+2003A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197613873 | ||||||
| chr2:197613912
|
G | T | 2 | a0001c0001t0009g0051a0001c0001t0009g0053 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1154+1964C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197613912 | ||||||
| chr2:197614029
|
T | C | 1 | a0001c0002t0001g0242 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1154+1847A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614029 | ||||||
| chr2:197614049
|
T | C | 1 | a0001c0002t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1154+1827A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614049 | ||||||
| chr2:197614287
|
C | T | 3 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1154+1589G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614287 | ||||||
| chr2:197614496
|
G | C | 1 | a0001c0001t0002g0297 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1154+1380C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614496 | ||||||
| chr2:197614614
|
C | T | 2 | a0001c0001t0014g0014a0001c0001t0014g0019 | 2 | NA18957.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1154+1262G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614614 | ||||||
| chr2:197614629
|
G | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1154+1247C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614629 | ||||||
| chr2:197614855
|
G | T | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1154+1021C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614855 | ||||||
| chr2:197614950
|
C | T | 5 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(2): Show | 7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1154+926G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197614950 | ||||||
| chr2:197615331
|
A | G | 1 | a0001c0001t0002g0184 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1154+545T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615331 | ||||||
| chr2:197615348
|
G | A | 194 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1154+528C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615348 | ||||||
| chr2:197615371
|
T | C | 1 | a0001c0001t0008g0005 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1154+505A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615371 | ||||||
| chr2:197615584
|
GT | G | 73 | a0001c0001t0002g0193a0001c0001t0003g0001a0001c0001t0003g0010others(70): Show | 74 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.1154+291delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615584 | ||||||
| chr2:197615654
|
G | A | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1154+222C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615654 | ||||||
| chr2:197615679
|
T | G | 2 | a0001c0001t0009g0051a0001c0001t0009g0053 | 2 | HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1154+197A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615679 | ||||||
| chr2:197615849
|
T | C | 2 | a0001c0001t0002g0178a0001c0001t0007g0177 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1154+27A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 7/8 | chr2 | 197615849 | ||||||
| chr2:197615986
|
G | C | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.1051-7C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197615986 | ||||||
| chr2:197616055
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1051-76G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616055 | ||||||
| chr2:197616131
|
A | G | 8 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(5): Show | 8 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1051-152T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616131 | ||||||
| chr2:197616135
|
T | C | 1 | a0001c0001t0002g0193 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1051-156A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616135 | ||||||
| chr2:197616243
|
A | G | 1 | a0001c0002t0001g0194 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1051-264T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616243 | ||||||
| chr2:197616268
|
C | CATTTT | 94 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0003g0002others(91): Show | 96 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.1051-294_1051-290d others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | ||||||
| chr2:197616268
|
C | CATTTTAT others(21): Show |
17 | a0001c0001t0002g0040a0001c0001t0002g0085a0001c0001t0002g0097others(14): Show | 17 | HG01243.hp2 HG01516.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.1051-290_1051-289i others(30): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | ||||||
| chr2:197616268
|
C | CATTTTAT others(26): Show |
65 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(62): Show | 65 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1051-290_1051-289i others(35): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | ||||||
| chr2:197616268
|
C | CATTTTAT others(31): Show |
34 | a0001c0001t0002g0083a0001c0001t0002g0114a0001c0001t0002g0120others(31): Show | 34 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1051-290_1051-289i others(40): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | ||||||
| chr2:197616268
|
C | CATTTTAT others(36): Show |
5 | a0001c0001t0003g0044a0001c0001t0005g0130a0001c0001t0008g0063others(2): Show | 5 | HG02083.hp2 HG02723.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051-290_1051-289i others(45): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | ||||||
| chr2:197616268
|
C | CATTTTAT others(3): Show |
1 | a0001c0001t0003g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1051-299_1051-290d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | ||||||
| chr2:197616268
|
C | CATTTTAT others(327): Show |
1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1051-290_1051-289i others(336): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616268 | ||||||
| chr2:197616269
|
A | ATTTTATT others(11): Show |
5 | a0001c0001t0003g0068a0001c0001t0006g0156a0001c0001t0006g0157others(2): Show | 5 | HG00639.hp1 HG01884.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051-291_1051-290i others(20): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616269 | ||||||
| chr2:197616274
|
A | ATTTATTT others(5): Show |
4 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(1): Show | 4 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1051-296_1051-295i others(14): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616274 | ||||||
| chr2:197616274
|
A | ATTTATTT others(6): Show |
9 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0143others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051-296_1051-295i others(15): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616274 | ||||||
| chr2:197616274
|
A | ATTTATTT others(5): Show |
1 | a0001c0001t0013g0054 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1051-296_1051-295i others(14): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616274 | ||||||
| chr2:197616275
|
T | TTTATTTT others(1): Show |
59 | a0001c0001t0002g0193a0001c0001t0002g0297a0001c0001t0003g0001others(56): Show | 60 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.1051-297_1051-296i others(10): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616275 | ||||||
| chr2:197616305
|
T | TTTATTTT others(1): Show |
120 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1051-327_1051-326i others(10): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616305 | ||||||
| chr2:197616309
|
A | ATTTATTT others(6): Show |
14 | a0001c0001t0002g0094a0001c0001t0002g0095a0001c0001t0002g0143others(11): Show | 14 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1051-331_1051-330i others(15): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616309 | ||||||
| chr2:197616309
|
A | ATTTTATT others(16): Show |
12 | a0001c0001t0003g0001a0001c0001t0003g0011a0001c0001t0003g0015others(9): Show | 13 | HG02132.hp2 HG02300.hp2 HG03209.hp2 others(10): Show |
intron_variant | MODIFIER | c.1051-331_1051-330i others(25): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616309 | ||||||
| chr2:197616309
|
A | ATTTTATT others(21): Show |
46 | a0001c0001t0002g0297a0001c0001t0003g0010a0001c0001t0003g0016others(43): Show | 46 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.1051-331_1051-330i others(30): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616309 | ||||||
| chr2:197616309
|
A | ATTTTATT others(26): Show |
5 | a0001c0001t0002g0193a0001c0001t0003g0168a0001c0001t0003g0176others(2): Show | 5 | HG01070.hp2 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051-331_1051-330i others(35): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616309 | ||||||
| chr2:197616309
|
A | ATTTTATT others(36): Show |
1 | a0001c0001t0003g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1051-331_1051-330i others(45): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616309 | ||||||
| chr2:197616309
|
A | T | 121 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1051-330T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616309 | ||||||
| chr2:197616311
|
A | T | 199 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1051-332T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616311 | ||||||
| chr2:197616412
|
C | T | 5 | a0001c0001t0002g0043a0001c0001t0002g0055a0001c0001t0002g0056others(2): Show | 5 | HG01243.hp2 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051-433G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616412 | ||||||
| chr2:197616453
|
G | A | 11 | a0001c0001t0002g0043a0001c0001t0002g0055a0001c0001t0002g0056others(8): Show | 11 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1051-474C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616453 | ||||||
| chr2:197616551
|
T | A | 1 | a0001c0001t0002g0143 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1051-572A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616551 | ||||||
| chr2:197616653
|
T | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1051-674A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616653 | ||||||
| chr2:197616732
|
G | A | 1 | a0001c0001t0029g0207 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1051-753C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616732 | ||||||
| chr2:197616928
|
C | A | 4 | a0001c0001t0003g0078a0001c0001t0003g0181a0001c0001t0003g0185others(1): Show | 4 | HG02630.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1050+872G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197616928 | ||||||
| chr2:197617024
|
G | A | 2 | a0001c0002t0001g0228a0001c0002t0001g0230 | 2 | HG01099.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1050+776C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617024 | ||||||
| chr2:197617140
|
A | C | 1 | a0001c0001t0002g0133 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1050+660T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617140 | ||||||
| chr2:197617247
|
C | A | 1 | a0001c0001t0003g0168 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1050+553G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617247 | ||||||
| chr2:197617258
|
G | A | 5 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(2): Show | 7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1050+542C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617258 | ||||||
| chr2:197617364
|
C | T | 1 | a0001c0001t0022g0091 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1050+436G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617364 | ||||||
| chr2:197617478
|
A | G | 1 | a0001c0001t0019g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1050+322T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617478 | ||||||
| chr2:197617498
|
C | T | 2 | a0001c0001t0017g0146a0001c0001t0017g0147 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1050+302G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 6/8 | chr2 | 197617498 | ||||||
| chr2:197618000
|
CAT | C | 8 | a0001c0001t0003g0160a0001c0001t0007g0084a0001c0001t0012g0142others(5): Show | 8 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.929-81_929-80delAT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618000 | ||||||
| chr2:197618061
|
C | CCCCTCT | 6 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(3): Show | 8 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.929-146_929-141dup others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618061 | ||||||
| chr2:197618211
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.929-290C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618211 | ||||||
| chr2:197618246
|
T | A | 1 | a0001c0002t0001g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.929-325A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618246 | ||||||
| chr2:197618319
|
C | T | 1 | a0001c0002t0001g0237 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.929-398G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618319 | ||||||
| chr2:197618327
|
A | G | 5 | a0001c0001t0003g0160a0001c0001t0012g0142a0001c0001t0012g0163others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.929-406T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618327 | ||||||
| chr2:197618371
|
G | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.929-450C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618371 | ||||||
| chr2:197618454
|
A | C | 1 | a0001c0001t0002g0048 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.929-533T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618454 | ||||||
| chr2:197618490
|
C | T | 121 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.929-569G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618490 | ||||||
| chr2:197618493
|
C | T | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.929-572G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618493 | ||||||
| chr2:197618506
|
A | AC | 8 | a0001c0001t0002g0305a0001c0002t0001g0211a0001c0002t0001g0222others(5): Show | 8 | HG00621.hp1 HG00738.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.929-586dupG | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618506 | ||||||
| chr2:197618568
|
C | G | 3 | a0001c0001t0013g0054a0001c0001t0013g0072a0001c0001t0013g0107 | 3 | HG02818.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.929-647G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618568 | ||||||
| chr2:197618665
|
A | C | 1 | a0001c0001t0002g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.929-744T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618665 | ||||||
| chr2:197618690
|
T | G | 1 | a0001c0001t0003g0022 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.929-769A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618690 | ||||||
| chr2:197618734
|
T | C | 2 | a0001c0002t0001g0257a0001c0002t0033g0231 | 2 | HG01168.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.929-813A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618734 | ||||||
| chr2:197618738
|
G | A | 1 | a0001c0001t0007g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.929-817C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618738 | ||||||
| chr2:197618743
|
G | A | 2 | a0001c0002t0001g0257a0001c0002t0033g0231 | 2 | HG01168.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.929-822C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618743 | ||||||
| chr2:197618746
|
C | T | 2 | a0001c0002t0001g0257a0001c0002t0033g0231 | 2 | HG01168.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.929-825G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618746 | ||||||
| chr2:197618774
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.929-853G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618774 | ||||||
| chr2:197618791
|
G | A | 1 | a0001c0001t0021g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.929-870C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618791 | ||||||
| chr2:197618859
|
C | A | 2 | a0001c0001t0015g0047a0001c0001t0015g0155 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.929-938G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618859 | ||||||
| chr2:197618875
|
A | C | 2 | a0001c0001t0015g0047a0001c0001t0015g0155 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.929-954T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618875 | ||||||
| chr2:197618879
|
C | T | 15 | a0001c0001t0001g0125a0001c0001t0005g0041a0001c0001t0005g0080others(12): Show | 15 | HG02027.hp1 HG02083.hp2 NA18940.hp2 others(12): Show |
intron_variant | MODIFIER | c.929-958G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618879 | ||||||
| chr2:197618943
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.929-1022G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618943 | ||||||
| chr2:197618955
|
G | T | 20 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0002t0001g0189others(17): Show | 20 | HG00621.hp1 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.929-1034C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618955 | ||||||
| chr2:197618975
|
C | T | 1 | a0001c0002t0001g0278 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.929-1054G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197618975 | ||||||
| chr2:197619106
|
C | T | 9 | a0001c0001t0002g0143a0001c0001t0002g0153a0001c0001t0003g0068others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.929-1185G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619106 | ||||||
| chr2:197619115
|
G | A | 1 | a0001c0002t0004g0188 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.929-1194C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619115 | ||||||
| chr2:197619121
|
T | C | 1 | a0001c0001t0002g0143 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.929-1200A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619121 | ||||||
| chr2:197619124
|
G | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.929-1203C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619124 | ||||||
| chr2:197619153
|
A | G | 206 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(203): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.929-1232T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619153 | ||||||
| chr2:197619180
|
C | T | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.929-1259G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619180 | ||||||
| chr2:197619243
|
A | G | 73 | a0001c0001t0002g0193a0001c0001t0003g0001a0001c0001t0003g0010others(70): Show | 74 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.929-1322T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619243 | ||||||
| chr2:197619248
|
A | G | 73 | a0001c0001t0002g0193a0001c0001t0003g0001a0001c0001t0003g0010others(70): Show | 74 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.929-1327T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619248 | ||||||
| chr2:197619250
|
A | G | 73 | a0001c0001t0002g0193a0001c0001t0003g0001a0001c0001t0003g0010others(70): Show | 74 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.929-1329T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619250 | ||||||
| chr2:197619291
|
A | G | 11 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.929-1370T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619291 | ||||||
| chr2:197619334
|
G | C | 5 | a0001c0001t0003g0160a0001c0001t0012g0142a0001c0001t0012g0163others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.929-1413C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619334 | ||||||
| chr2:197619371
|
G | C | 121 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.929-1450C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619371 | ||||||
| chr2:197619395
|
C | T | 1 | a0001c0001t0002g0089 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.929-1474G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619395 | ||||||
| chr2:197619715
|
C | T | 1 | a0001c0001t0003g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.929-1794G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619715 | ||||||
| chr2:197619740
|
T | TA | 82 | a0001c0001t0001g0125a0001c0001t0002g0040a0001c0001t0002g0042others(79): Show | 82 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.929-1820dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619740 | ||||||
| chr2:197619740
|
TA | T | 11 | a0001c0001t0012g0190a0001c0002t0001g0217a0001c0002t0001g0218others(8): Show | 11 | HG02056.hp1 HG02486.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.929-1820delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619740 | ||||||
| chr2:197619750
|
A | T | 1 | a0001c0001t0003g0031 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.929-1829T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619750 | ||||||
| chr2:197619751
|
AAT | A | 8 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(5): Show | 8 | HG02886.hp1 HG02896.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.929-1832_929-1831d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619751 | ||||||
| chr2:197619752
|
AT | A | 14 | a0001c0001t0002g0143a0001c0001t0002g0307a0001c0001t0003g0050others(11): Show | 14 | HG01081.hp2 HG01515.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.929-1832delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619752 | ||||||
| chr2:197619753
|
T | A | 122 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.929-1832A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619753 | ||||||
| chr2:197619753
|
T | TA | 5 | a0001c0001t0003g0068a0001c0001t0009g0051a0001c0001t0009g0052others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.929-1833dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619753 | ||||||
| chr2:197619756
|
T | A | 15 | a0001c0001t0002g0077a0001c0001t0002g0140a0001c0001t0002g0166others(12): Show | 15 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.929-1835A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619756 | ||||||
| chr2:197619759
|
T | A | 1 | a0001c0001t0002g0111 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.929-1838A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619759 | ||||||
| chr2:197619762
|
C | T | 199 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.929-1841G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619762 | ||||||
| chr2:197619777
|
A | G | 9 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(6): Show | 9 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.929-1856T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619777 | ||||||
| chr2:197619865
|
CT | C | 7 | a0001c0001t0002g0074a0001c0001t0002g0119a0001c0001t0003g0050others(4): Show | 7 | HG01515.hp2 HG02015.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.929-1945delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197619865 | ||||||
| chr2:197620174
|
C | T | 1 | a0001c0001t0012g0191 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.929-2253G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620174 | ||||||
| chr2:197620458
|
C | T | 1 | a0001c0001t0021g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.929-2537G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620458 | ||||||
| chr2:197620617
|
A | C | 206 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(203): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.929-2696T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620617 | ||||||
| chr2:197620834
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.929-2913G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620834 | ||||||
| chr2:197620959
|
C | G | 1 | a0001c0002t0007g0232 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.929-3038G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620959 | ||||||
| chr2:197620996
|
A | C | 1 | a0001c0001t0002g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.929-3075T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620996 | ||||||
| chr2:197620997
|
AAAAC | A | 8 | a0001c0001t0002g0128a0001c0001t0002g0166a0001c0001t0002g0186others(5): Show | 8 | HG00639.hp1 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.929-3080_929-3077d others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197620997 | ||||||
| chr2:197621174
|
C | T | 1 | a0001c0001t0003g0010 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.929-3253G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621174 | ||||||
| chr2:197621257
|
T | C | 1 | a0001c0001t0002g0143 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.929-3336A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621257 | ||||||
| chr2:197621401
|
G | GT | 8 | a0001c0001t0002g0043a0001c0001t0002g0140a0001c0001t0003g0031others(5): Show | 8 | HG00323.hp2 HG02965.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.929-3481dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621401 | ||||||
| chr2:197621401
|
G | GTT | 179 | a0001c0001t0001g0125a0001c0001t0002g0039a0001c0001t0002g0040others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.929-3482_929-3481d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621401 | ||||||
| chr2:197621401
|
G | GTTT | 15 | a0001c0001t0002g0038a0001c0001t0002g0067a0001c0001t0002g0074others(12): Show | 15 | HG02055.hp1 HG02145.hp2 HG02886.hp2 others(12): Show |
intron_variant | MODIFIER | c.929-3483_929-3481d others(5): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621401 | ||||||
| chr2:197621510
|
A | G | 2 | a0001c0001t0002g0120a0001c0007t0002g0086 | 2 | HG04228.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.929-3589T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621510 | ||||||
| chr2:197621615
|
C | T | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.929-3694G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621615 | ||||||
| chr2:197621881
|
A | T | 1 | a0001c0001t0003g0070 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.929-3960T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197621881 | ||||||
| chr2:197622383
|
C | T | 1 | a0001c0002t0003g0200 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.929-4462G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622383 | ||||||
| chr2:197622494
|
C | T | 1 | a0001c0002t0032g0271 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.929-4573G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622494 | ||||||
| chr2:197622504
|
C | T | 1 | a0001c0002t0001g0262 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.929-4583G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622504 | ||||||
| chr2:197622554
|
C | T | 199 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.929-4633G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622554 | ||||||
| chr2:197622604
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.929-4683G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622604 | ||||||
| chr2:197622647
|
T | A | 2 | a0001c0001t0003g0171a0001c0001t0006g0170 | 2 | NA18985.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.929-4726A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622647 | ||||||
| chr2:197622721
|
G | A | 5 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(2): Show | 7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.929-4800C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622721 | ||||||
| chr2:197622896
|
C | G | 5 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(2): Show | 7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.929-4975G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197622896 | ||||||
| chr2:197623048
|
C | G | 1 | a0001c0001t0006g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.929-5127G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623048 | ||||||
| chr2:197623230
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.929-5309T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623230 | ||||||
| chr2:197623627
|
C | T | 1 | a0001c0001t0006g0156 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.929-5706G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623627 | ||||||
| chr2:197623698
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.929-5777G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623698 | ||||||
| chr2:197623744
|
G | C | 121 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.929-5823C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623744 | ||||||
| chr2:197623915
|
C | T | 2 | a0001c0002t0001g0244a0001c0002t0001g0245 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.929-5994G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623915 | ||||||
| chr2:197623916
|
G | A | 2 | a0001c0001t0026g0006a0001c0002t0001g0265 | 2 | HG00738.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.929-5995C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623916 | ||||||
| chr2:197623961
|
G | T | 1 | a0001c0001t0010g0209 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.929-6040C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197623961 | ||||||
| chr2:197624050
|
C | T | 1 | a0001c0002t0001g0218 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.929-6129G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624050 | ||||||
| chr2:197624172
|
G | T | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.929-6251C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624172 | ||||||
| chr2:197624346
|
T | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.929-6425A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624346 | ||||||
| chr2:197624374
|
C | T | 3 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0260 | 3 | NA18977.hp1 NA19075.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.929-6453G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624374 | ||||||
| chr2:197624375
|
G | A | 1 | a0001c0002t0004g0292 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.929-6454C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624375 | ||||||
| chr2:197624389
|
G | T | 2 | a0001c0001t0003g0160a0001c0001t0012g0163 | 2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.929-6468C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624389 | ||||||
| chr2:197624395
|
G | C | 1 | a0001c0001t0007g0084 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.929-6474C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624395 | ||||||
| chr2:197624484
|
G | A | 1 | a0001c0001t0007g0098 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.928+6527C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624484 | ||||||
| chr2:197624522
|
C | T | 1 | a0001c0001t0005g0106 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.928+6489G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624522 | ||||||
| chr2:197624529
|
C | T | 199 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.928+6482G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624529 | ||||||
| chr2:197624585
|
G | A | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.928+6426C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624585 | ||||||
| chr2:197624597
|
C | CA | 18 | a0001c0001t0002g0090a0001c0001t0004g0144a0001c0001t0004g0145others(15): Show | 18 | HG00673.hp2 HG01346.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.928+6413dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624597 | ||||||
| chr2:197624597
|
CA | C | 165 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(162): Show | 168 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.928+6413delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624597 | ||||||
| chr2:197624597
|
CAA | C | 12 | a0001c0001t0002g0043a0001c0001t0003g0299a0001c0001t0005g0041others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.928+6412_928+6413d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624597 | ||||||
| chr2:197624597
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.928+6402_928+6413d others(14): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624597 | ||||||
| chr2:197624616
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.928+6395T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624616 | ||||||
| chr2:197624636
|
A | T | 1 | a0001c0001t0016g0126 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.928+6375T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624636 | ||||||
| chr2:197624687
|
C | T | 9 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(6): Show | 9 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.928+6324G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624687 | ||||||
| chr2:197624861
|
A | G | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.928+6150T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624861 | ||||||
| chr2:197624883
|
A | G | 121 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.928+6128T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624883 | ||||||
| chr2:197624888
|
G | A | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.928+6123C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197624888 | ||||||
| chr2:197625101
|
T | G | 1 | a0001c0001t0003g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.928+5910A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625101 | ||||||
| chr2:197625473
|
C | T | 2 | a0001c0001t0008g0063a0001c0001t0011g0059 | 2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.928+5538G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625473 | ||||||
| chr2:197625491
|
A | G | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+5520T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625491 | ||||||
| chr2:197625663
|
T | TCTCTC | 8 | a0001c0001t0003g0024a0001c0001t0003g0029a0001c0001t0003g0148others(5): Show | 9 | HG01891.hp1 HG02015.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.928+5343_928+5347d others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | ||||||
| chr2:197625663
|
T | TCTCTCCT others(3): Show |
6 | a0001c0001t0003g0002a0001c0001t0003g0149a0001c0001t0008g0004others(3): Show | 7 | HG02109.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.928+5338_928+5347d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | ||||||
| chr2:197625663
|
T | TCTCTCCT others(8): Show |
5 | a0001c0001t0003g0173a0001c0001t0006g0158a0001c0001t0008g0008others(2): Show | 5 | HG02165.hp1 HG04199.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.928+5333_928+5347d others(17): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | ||||||
| chr2:197625663
|
T | TCTCTCCT others(13): Show |
2 | a0001c0001t0003g0174a0001c0001t0008g0007 | 2 | HG00408.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.928+5328_928+5347d others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | ||||||
| chr2:197625663
|
TCTCTC | T | 83 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0003g0017others(80): Show | 83 | HG00323.hp1 HG00621.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.928+5343_928+5347d others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | ||||||
| chr2:197625663
|
TCTCTCCT others(3): Show |
T | 20 | a0001c0001t0003g0011a0001c0001t0003g0044a0001c0001t0003g0045others(17): Show | 20 | HG00735.hp1 HG01106.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.928+5338_928+5347d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | ||||||
| chr2:197625663
|
TCTCTCCT others(8): Show |
T | 5 | a0001c0001t0003g0069a0001c0001t0003g0160a0001c0001t0012g0142others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+5333_928+5347d others(17): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | ||||||
| chr2:197625663
|
TCTCTCCT others(13): Show |
T | 1 | a0001c0002t0001g0223 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.928+5328_928+5347d others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625663 | ||||||
| chr2:197625699
|
C | CTCTCCTC others(23): Show |
4 | a0001c0001t0002g0079a0001c0001t0007g0084a0001c0001t0009g0141others(1): Show | 4 | HG02809.hp1 HG02970.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+5311_928+5312i others(32): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625699 | ||||||
| chr2:197625699
|
C | CTCTCCTC others(18): Show |
6 | a0001c0001t0001g0125a0001c0001t0002g0119a0001c0001t0003g0068others(3): Show | 6 | HG01884.hp1 HG02027.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+5311_928+5312i others(27): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625699 | ||||||
| chr2:197625699
|
C | CTCTCCTC others(13): Show |
82 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(79): Show | 82 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.928+5311_928+5312i others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625699 | ||||||
| chr2:197625699
|
C | CTCTCCTC others(8): Show |
21 | a0001c0001t0002g0048a0001c0001t0002g0095a0001c0001t0002g0128others(18): Show | 21 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.928+5311_928+5312i others(17): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625699 | ||||||
| chr2:197625699
|
C | CTCTCCTC others(3): Show |
8 | a0001c0001t0002g0186a0001c0001t0010g0206a0001c0001t0010g0208others(5): Show | 8 | HG01168.hp2 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.928+5311_928+5312i others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625699 | ||||||
| chr2:197625729
|
T | C | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.928+5282A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625729 | ||||||
| chr2:197625731
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.928+5280G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625731 | ||||||
| chr2:197625983
|
T | G | 1 | a0001c0001t0003g0018 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.928+5028A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625983 | ||||||
| chr2:197625989
|
G | A | 3 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157 | 3 | HG02886.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.928+5022C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197625989 | ||||||
| chr2:197626014
|
C | G | 1 | a0001c0001t0003g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928+4997G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626014 | ||||||
| chr2:197626026
|
T | G | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+4985A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626026 | ||||||
| chr2:197626078
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.928+4933G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626078 | ||||||
| chr2:197626376
|
G | A | 3 | a0001c0002t0001g0009a0001c0002t0001g0199a0001c0002t0001g0223 | 3 | HG00558.hp2 HG02165.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.928+4635C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626376 | ||||||
| chr2:197626386
|
C | T | 200 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(197): Show | 201 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.928+4625G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626386 | ||||||
| chr2:197626456
|
C | T | 116 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.928+4555G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626456 | ||||||
| chr2:197626526
|
T | G | 1 | a0001c0001t0003g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.928+4485A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626526 | ||||||
| chr2:197626562
|
C | CAAAT | 5 | a0001c0001t0003g0160a0001c0001t0012g0142a0001c0001t0012g0163others(2): Show | 5 | HG02145.hp2 HG02486.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+4445_928+4448d others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | ||||||
| chr2:197626562
|
C | CAAATAAA others(1): Show |
175 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.928+4441_928+4448d others(10): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | ||||||
| chr2:197626562
|
C | CAAATAAA others(5): Show |
18 | a0001c0001t0002g0297a0001c0001t0003g0002a0001c0001t0003g0104others(15): Show | 20 | HG01243.hp1 HG01261.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.928+4437_928+4448d others(14): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | ||||||
| chr2:197626562
|
C | CAAATAAA others(9): Show |
4 | a0001c0001t0002g0137a0001c0001t0002g0143a0001c0001t0002g0153others(1): Show | 4 | HG02015.hp2 HG02280.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+4433_928+4448d others(18): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | ||||||
| chr2:197626562
|
C | CAAATAAA others(13): Show |
2 | a0001c0001t0006g0156a0001c0001t0006g0157 | 2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.928+4429_928+4448d others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | ||||||
| chr2:197626562
|
C | CAAATAAA others(17): Show |
1 | a0001c0001t0006g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.928+4425_928+4448d others(26): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | ||||||
| chr2:197626562
|
CAAAT | C | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+4445_928+4448d others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626562 | ||||||
| chr2:197626614
|
C | CT | 75 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0040others(72): Show | 75 | HG00408.hp2 HG00558.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.928+4396dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626614 | ||||||
| chr2:197626614
|
C | CTT | 19 | a0001c0001t0002g0039a0001c0001t0002g0085a0001c0001t0002g0096others(16): Show | 19 | HG00621.hp2 HG01243.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.928+4395_928+4396d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626614 | ||||||
| chr2:197626614
|
C | CTTT | 7 | a0001c0001t0002g0109a0001c0001t0002g0116a0001c0001t0010g0206others(4): Show | 7 | HG01891.hp2 HG02148.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.928+4396_928+4397i others(5): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626614 | ||||||
| chr2:197626617
|
C | CT | 10 | a0001c0001t0003g0002a0001c0001t0003g0070a0001c0001t0003g0148others(7): Show | 12 | HG01261.hp1 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.928+4393dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626617 | ||||||
| chr2:197626617
|
C | CTT | 64 | a0001c0001t0003g0001a0001c0001t0003g0011a0001c0001t0003g0015others(61): Show | 65 | HG00323.hp2 HG00408.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.928+4392_928+4393d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626617 | ||||||
| chr2:197626617
|
C | CTTT | 15 | a0001c0001t0002g0193a0001c0001t0003g0010a0001c0001t0003g0017others(12): Show | 15 | HG01361.hp1 HG02055.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.928+4391_928+4393d others(5): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626617 | ||||||
| chr2:197626617
|
C | T | 120 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.928+4394G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626617 | ||||||
| chr2:197626617
|
CT | C | 81 | a0001c0001t0001g0161a0001c0002t0001g0009a0001c0002t0001g0139others(78): Show | 81 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.928+4393delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626617 | ||||||
| chr2:197626756
|
C | G | 2 | a0001c0001t0002g0075a0001c0001t0007g0073 | 2 | HG00621.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.928+4255G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626756 | ||||||
| chr2:197626767
|
C | G | 1 | a0001c0002t0001g0298 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.928+4244G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626767 | ||||||
| chr2:197626784
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.928+4227G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197626784 | ||||||
| chr2:197627105
|
G | A | 1 | a0001c0001t0011g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.928+3906C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627105 | ||||||
| chr2:197627191
|
C | T | 1 | a0001c0002t0001g0222 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.928+3820G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627191 | ||||||
| chr2:197627592
|
T | G | 131 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.928+3419A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627592 | ||||||
| chr2:197627622
|
T | C | 3 | a0001c0001t0002g0153a0001c0001t0012g0191a0001c0001t0021g0037 | 3 | HG02280.hp2 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.928+3389A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627622 | ||||||
| chr2:197627647
|
G | C | 2 | a0001c0001t0008g0007a0001c0001t0008g0008 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.928+3364C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627647 | ||||||
| chr2:197627694
|
G | A | 1 | a0001c0001t0007g0098 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.928+3317C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627694 | ||||||
| chr2:197627874
|
C | T | 67 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0079others(64): Show | 68 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.928+3137G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627874 | ||||||
| chr2:197627875
|
G | C | 1 | a0001c0001t0005g0080 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.928+3136C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627875 | ||||||
| chr2:197627883
|
G | A | 2 | a0001c0001t0002g0042a0001c0001t0002g0132 | 2 | NA18961.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.928+3128C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627883 | ||||||
| chr2:197627883
|
G | C | 1 | a0001c0002t0004g0226 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.928+3128C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627883 | ||||||
| chr2:197627883
|
G | GC | 12 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0003g0025others(9): Show | 12 | HG01192.hp1 HG01934.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.928+3127dupG | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627883 | ||||||
| chr2:197627885
|
C | G | 1 | a0001c0001t0006g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.928+3126G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627885 | ||||||
| chr2:197627911
|
T | C | 1 | a0001c0002t0001g0252 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.928+3100A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197627911 | ||||||
| chr2:197628102
|
C | T | 66 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(63): Show | 67 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.928+2909G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628102 | ||||||
| chr2:197628103
|
C | T | 66 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(63): Show | 67 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.928+2908G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628103 | ||||||
| chr2:197628113
|
C | T | 124 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(121): Show | 126 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.928+2898G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628113 | ||||||
| chr2:197628180
|
C | CT | 66 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(63): Show | 67 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.928+2830dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628180 | ||||||
| chr2:197628219
|
T | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.928+2792A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628219 | ||||||
| chr2:197628313
|
G | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0031 | 2 | HG00323.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.928+2698C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628313 | ||||||
| chr2:197628343
|
G | A | 6 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(3): Show | 6 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.928+2668C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628343 | ||||||
| chr2:197628362
|
C | T | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.928+2649G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628362 | ||||||
| chr2:197628616
|
GA | G | 66 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(63): Show | 67 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.928+2394delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628616 | ||||||
| chr2:197628758
|
G | A | 1 | a0001c0002t0001g0298 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.928+2253C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628758 | ||||||
| chr2:197628880
|
C | T | 3 | a0001c0002t0001g0270a0001c0002t0004g0291a0001c0002t0032g0271 | 3 | HG01993.hp1 HG02004.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.928+2131G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628880 | ||||||
| chr2:197628979
|
T | A | 115 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(112): Show | 117 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.928+2032A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197628979 | ||||||
| chr2:197629002
|
G | A | 1 | a0001c0001t0029g0207 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.928+2009C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629002 | ||||||
| chr2:197629094
|
C | G | 66 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(63): Show | 67 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.928+1917G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629094 | ||||||
| chr2:197629165
|
A | G | 1 | a0001c0001t0004g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.928+1846T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629165 | ||||||
| chr2:197629245
|
C | T | 2 | a0001c0001t0002g0153a0001c0001t0021g0037 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.928+1766G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629245 | ||||||
| chr2:197629282
|
C | A | 66 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(63): Show | 67 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.928+1729G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629282 | ||||||
| chr2:197629341
|
A | C | 99 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.928+1670T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629341 | ||||||
| chr2:197629387
|
C | T | 202 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.928+1624G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629387 | ||||||
| chr2:197629466
|
G | T | 1 | a0001c0002t0001g0230 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.928+1545C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629466 | ||||||
| chr2:197629560
|
A | G | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.928+1451T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629560 | ||||||
| chr2:197629622
|
G | C | 1 | a0001c0001t0002g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.928+1389C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629622 | ||||||
| chr2:197629675
|
T | TAC | 14 | a0001c0001t0002g0112a0001c0001t0002g0143a0001c0001t0003g0057others(11): Show | 14 | HG01258.hp2 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.928+1334_928+1335d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | ||||||
| chr2:197629675
|
T | TACAC | 14 | a0001c0001t0002g0178a0001c0001t0003g0044a0001c0001t0003g0045others(11): Show | 14 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.928+1332_928+1335d others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | ||||||
| chr2:197629675
|
T | TACACAC | 9 | a0001c0001t0008g0004a0001c0001t0008g0063a0001c0001t0010g0208others(6): Show | 9 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.928+1330_928+1335d others(8): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | ||||||
| chr2:197629675
|
T | TACACACA others(3): Show |
13 | a0001c0001t0002g0166a0001c0001t0003g0050a0001c0001t0003g0152others(10): Show | 13 | HG01069.hp1 HG01106.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.928+1326_928+1335d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | ||||||
| chr2:197629675
|
T | TACACACA others(5): Show |
3 | a0001c0001t0003g0176a0001c0001t0006g0158a0004c0005t0006g0159 | 3 | HG01070.hp2 HG01516.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.928+1324_928+1335d others(14): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | ||||||
| chr2:197629675
|
T | TACACACA others(7): Show |
24 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0193others(21): Show | 24 | HG00323.hp2 HG00408.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.928+1322_928+1335d others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | ||||||
| chr2:197629675
|
T | TACACACA others(9): Show |
5 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0032others(2): Show | 5 | HG02083.hp1 HG02145.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+1320_928+1335d others(18): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | ||||||
| chr2:197629675
|
T | TACACACA others(11): Show |
6 | a0001c0001t0003g0001a0001c0001t0003g0027a0001c0001t0003g0028others(3): Show | 7 | HG02886.hp2 NA18939.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.928+1318_928+1335d others(20): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | ||||||
| chr2:197629675
|
T | TACACACA others(13): Show |
3 | a0001c0001t0003g0018a0001c0001t0015g0047a0001c0001t0015g0155 | 3 | HG02717.hp2 HG03139.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.928+1316_928+1335d others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | ||||||
| chr2:197629675
|
T | TACACACA others(15): Show |
2 | a0001c0001t0006g0156a0001c0001t0006g0157 | 2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.928+1314_928+1335d others(24): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | ||||||
| chr2:197629675
|
TAC | T | 6 | a0001c0001t0002g0297a0001c0001t0003g0002a0001c0001t0003g0148others(3): Show | 8 | HG01261.hp1 HG01884.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.928+1334_928+1335d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629675 | ||||||
| chr2:197629696
|
A | ACACACAC others(13): Show |
1 | a0001c0001t0021g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.928+1314_928+1315i others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629696 | ||||||
| chr2:197629696
|
A | ACACACAC others(9): Show |
1 | a0001c0001t0002g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.928+1314_928+1315i others(18): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629696 | ||||||
| chr2:197629697
|
C | T | 2 | a0001c0002t0001g0244a0001c0002t0001g0245 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.928+1314G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629697 | ||||||
| chr2:197629699
|
C | T | 3 | a0001c0002t0001g0244a0001c0002t0001g0245a0001c0002t0001g0266 | 3 | HG01192.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.928+1312G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629699 | ||||||
| chr2:197629700
|
A | T | 2 | a0001c0002t0001g0244a0001c0002t0001g0245 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.928+1311T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629700 | ||||||
| chr2:197629701
|
T | C | 101 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.928+1310A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629701 | ||||||
| chr2:197629702
|
A | ACACATAT others(4): Show |
2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.928+1308_928+1309i others(13): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629702 | ||||||
| chr2:197629702
|
A | ATATTTAT | 98 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.928+1308_928+1309i others(9): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629702 | ||||||
| chr2:197629702
|
A | ATTTAT | 84 | a0001c0002t0001g0009a0001c0002t0001g0139a0001c0002t0001g0189others(81): Show | 84 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.928+1304_928+1308d others(7): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629702 | ||||||
| chr2:197629702
|
A | ATTTATTT others(3): Show |
15 | a0001c0002t0001g0222a0001c0002t0001g0246a0001c0002t0001g0247others(12): Show | 15 | HG00621.hp1 HG01928.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.928+1299_928+1308d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629702 | ||||||
| chr2:197629702
|
A | ATTTATTT others(8): Show |
3 | a0001c0002t0002g0196a0001c0002t0002g0197a0001c0002t0002g0286 | 3 | NA18946.hp2 NA18951.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.928+1294_928+1308d others(17): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629702 | ||||||
| chr2:197629702
|
A | T | 1 | a0001c0002t0001g0266 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.928+1309T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629702 | ||||||
| chr2:197629731
|
A | T | 5 | a0001c0001t0008g0063a0001c0001t0011g0059a0001c0001t0011g0060others(2): Show | 5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.928+1280T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629731 | ||||||
| chr2:197629736
|
T | A | 9 | a0001c0002t0001g0222a0001c0002t0001g0246a0001c0002t0001g0247others(6): Show | 9 | HG00621.hp1 HG01928.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.928+1275A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629736 | ||||||
| chr2:197629744
|
A | G | 125 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(122): Show | 127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.928+1267T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629744 | ||||||
| chr2:197629777
|
T | C | 1 | a0001c0006t0006g0175 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.928+1234A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629777 | ||||||
| chr2:197629809
|
A | T | 3 | a0001c0001t0003g0057a0001c0001t0003g0071a0001c0001t0013g0072 | 3 | HG02818.hp2 HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.928+1202T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629809 | ||||||
| chr2:197629935
|
G | C | 6 | a0001c0001t0002g0297a0001c0001t0003g0002a0001c0001t0003g0148others(3): Show | 8 | HG01261.hp1 HG01884.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.928+1076C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197629935 | ||||||
| chr2:197630004
|
G | A | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.928+1007C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630004 | ||||||
| chr2:197630058
|
C | T | 56 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(53): Show | 57 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.928+953G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630058 | ||||||
| chr2:197630078
|
C | T | 1 | a0001c0002t0001g0294 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.928+933G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630078 | ||||||
| chr2:197630103
|
T | C | 5 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157others(2): Show | 5 | HG02717.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.928+908A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630103 | ||||||
| chr2:197630208
|
TAATA | T | 202 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.928+799_928+802del others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630208 | ||||||
| chr2:197630388
|
T | C | 1 | a0001c0001t0012g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.928+623A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630388 | ||||||
| chr2:197630535
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.928+476T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630535 | ||||||
| chr2:197630553
|
C | T | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.928+458G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630553 | ||||||
| chr2:197630696
|
C | T | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.928+315G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630696 | ||||||
| chr2:197630707
|
G | C | 125 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(122): Show | 127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.928+304C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630707 | ||||||
| chr2:197630858
|
A | G | 1 | a0001c0002t0001g0229 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.928+153T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 5/8 | chr2 | 197630858 | ||||||
| chr2:197631255
|
A | G | 5 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157others(2): Show | 5 | HG02717.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.719-35T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197631255 | ||||||
| chr2:197631322
|
G | A | 1 | a0001c0002t0001g0216 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.719-102C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197631322 | ||||||
| chr2:197631566
|
G | C | 1 | a0001c0002t0001g0255 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.719-346C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197631566 | ||||||
| chr2:197631605
|
T | C | 4 | a0001c0002t0001g0249a0001c0002t0001g0251a0001c0002t0001g0252others(1): Show | 4 | NA18944.hp1 NA18950.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.719-385A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197631605 | ||||||
| chr2:197631614
|
A | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.719-394T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197631614 | ||||||
| chr2:197631959
|
A | AC | 6 | a0001c0001t0005g0103a0001c0001t0007g0098a0001c0002t0001g0009others(3): Show | 6 | HG01099.hp1 HG01175.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.719-740dupG | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197631959 | ||||||
| chr2:197632003
|
A | G | 1 | a0001c0001t0003g0150 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.719-783T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632003 | ||||||
| chr2:197632027
|
A | C | 1 | a0001c0002t0001g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.719-807T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632027 | ||||||
| chr2:197632064
|
A | G | 3 | a0001c0002t0001g0267a0001c0002t0001g0268a0001c0002t0001g0294 | 3 | HG01928.hp2 HG01978.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.719-844T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632064 | ||||||
| chr2:197632381
|
C | T | 54 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0166others(51): Show | 55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.719-1161G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632381 | ||||||
| chr2:197632452
|
T | C | 2 | a0001c0001t0002g0153a0001c0001t0021g0037 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.719-1232A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632452 | ||||||
| chr2:197632525
|
T | C | 1 | a0001c0001t0003g0029 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.718+1193A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632525 | ||||||
| chr2:197632631
|
C | T | 1 | a0001c0001t0007g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.718+1087G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632631 | ||||||
| chr2:197632699
|
G | A | 5 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157others(2): Show | 5 | HG02717.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.718+1019C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632699 | ||||||
| chr2:197632788
|
T | G | 137 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.718+930A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632788 | ||||||
| chr2:197632985
|
C | T | 125 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(122): Show | 127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.718+733G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197632985 | ||||||
| chr2:197633008
|
G | T | 1 | a0001c0001t0002g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.718+710C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633008 | ||||||
| chr2:197633011
|
T | A | 1 | a0001c0002t0004g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.718+707A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633011 | ||||||
| chr2:197633022
|
A | T | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.718+696T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633022 | ||||||
| chr2:197633319
|
T | G | 5 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(2): Show | 7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.718+399A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633319 | ||||||
| chr2:197633328
|
A | T | 2 | a0002c0003t0001g0227a0002c0003t0001g0256 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.718+390T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633328 | ||||||
| chr2:197633536
|
A | G | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.718+182T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633536 | ||||||
| chr2:197633592
|
T | G | 202 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.718+126A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 4/8 | chr2 | 197633592 | ||||||
| chr2:197634050
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | NA18979.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.439-53A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634050 | ||||||
| chr2:197634061
|
A | G | 1 | a0001c0001t0021g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.439-64T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634061 | ||||||
| chr2:197634333
|
A | G | 1 | a0001c0001t0019g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.439-336T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634333 | ||||||
| chr2:197634438
|
C | T | 56 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(53): Show | 57 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.439-441G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634438 | ||||||
| chr2:197634692
|
ATTTTTTA others(4): Show |
A | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-706_439-696del others(11): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634692 | ||||||
| chr2:197634699
|
AT | A | 9 | a0001c0001t0002g0134a0001c0001t0003g0002a0001c0001t0003g0057others(6): Show | 11 | HG00408.hp2 HG01261.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.439-703delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634699 | ||||||
| chr2:197634703
|
T | A | 1 | a0001c0002t0001g0194 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.439-706A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634703 | ||||||
| chr2:197634720
|
ATTAT | A | 57 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(54): Show | 58 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.439-727_439-724del others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634720 | ||||||
| chr2:197634720
|
ATTATTTA others(1): Show |
A | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-731_439-724del others(8): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634720 | ||||||
| chr2:197634814
|
A | C | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-817T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634814 | ||||||
| chr2:197634832
|
C | A | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-835G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634832 | ||||||
| chr2:197634850
|
A | G | 1 | a0001c0002t0001g0194 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.439-853T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634850 | ||||||
| chr2:197634874
|
T | A | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-877A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634874 | ||||||
| chr2:197634977
|
A | T | 1 | a0001c0002t0001g0278 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.439-980T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634977 | ||||||
| chr2:197634983
|
G | A | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.439-986C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634983 | ||||||
| chr2:197634991
|
G | A | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.439-994C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634991 | ||||||
| chr2:197634991
|
G | GT | 125 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(122): Show | 127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.439-995dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197634991 | ||||||
| chr2:197635005
|
C | T | 59 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(56): Show | 60 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.439-1008G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635005 | ||||||
| chr2:197635128
|
G | T | 193 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(190): Show | 196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.439-1131C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635128 | ||||||
| chr2:197635167
|
T | A | 15 | a0001c0001t0001g0125a0001c0001t0005g0041a0001c0001t0005g0080others(12): Show | 15 | HG02027.hp1 HG02083.hp2 NA18940.hp2 others(12): Show |
intron_variant | MODIFIER | c.439-1170A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635167 | ||||||
| chr2:197635199
|
T | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.439-1202A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635199 | ||||||
| chr2:197635231
|
T | C | 137 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.439-1234A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635231 | ||||||
| chr2:197635294
|
T | A | 1 | a0001c0002t0004g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439-1297A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635294 | ||||||
| chr2:197635295
|
C | A | 1 | a0001c0002t0004g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439-1298G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635295 | ||||||
| chr2:197635296
|
C | A | 1 | a0001c0002t0004g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439-1299G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635296 | ||||||
| chr2:197635297
|
C | G | 1 | a0001c0002t0004g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439-1300G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635297 | ||||||
| chr2:197635299
|
G | C | 1 | a0001c0002t0004g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439-1302C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635299 | ||||||
| chr2:197635304
|
G | C | 1 | a0001c0002t0004g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439-1307C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635304 | ||||||
| chr2:197635326
|
C | T | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.439-1329G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635326 | ||||||
| chr2:197635342
|
C | T | 1 | a0001c0002t0001g0290 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.439-1345G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635342 | ||||||
| chr2:197635423
|
A | G | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-1426T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635423 | ||||||
| chr2:197635428
|
T | G | 1 | a0001c0001t0002g0183 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.439-1431A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635428 | ||||||
| chr2:197635511
|
A | G | 1 | a0001c0001t0009g0051 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.439-1514T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635511 | ||||||
| chr2:197635514
|
T | A | 1 | a0001c0001t0002g0112 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.439-1517A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635514 | ||||||
| chr2:197635546
|
T | G | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.439-1549A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635546 | ||||||
| chr2:197635553
|
T | C | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-1556A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635553 | ||||||
| chr2:197635637
|
G | C | 1 | a0001c0001t0003g0032 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.439-1640C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635637 | ||||||
| chr2:197635734
|
T | G | 1 | a0001c0002t0001g0250 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.439-1737A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635734 | ||||||
| chr2:197635951
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.439-1954G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635951 | ||||||
| chr2:197635972
|
C | G | 1 | a0001c0001t0003g0150 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.439-1975G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197635972 | ||||||
| chr2:197636030
|
C | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.439-2033G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636030 | ||||||
| chr2:197636055
|
C | T | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.439-2058G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636055 | ||||||
| chr2:197636083
|
T | C | 5 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157others(2): Show | 5 | HG02717.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.439-2086A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636083 | ||||||
| chr2:197636192
|
T | C | 1 | a0004c0005t0006g0159 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.439-2195A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636192 | ||||||
| chr2:197636242
|
G | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.439-2245C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636242 | ||||||
| chr2:197636293
|
T | G | 133 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(130): Show | 135 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.439-2296A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636293 | ||||||
| chr2:197636453
|
A | C | 3 | a0001c0002t0004g0225a0001c0002t0004g0226a0001c0002t0004g0260 | 3 | NA18977.hp1 NA19075.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.439-2456T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636453 | ||||||
| chr2:197636485
|
T | A | 5 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(2): Show | 7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.439-2488A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636485 | ||||||
| chr2:197636743
|
C | A | 2 | a0001c0002t0001g0267a0001c0002t0001g0268 | 2 | HG01928.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.439-2746G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636743 | ||||||
| chr2:197636763
|
C | A | 1 | a0001c0001t0002g0183 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.439-2766G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636763 | ||||||
| chr2:197636835
|
C | T | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.439-2838G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197636835 | ||||||
| chr2:197637053
|
T | C | 1 | a0001c0002t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.439-3056A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637053 | ||||||
| chr2:197637062
|
A | T | 202 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.439-3065T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637062 | ||||||
| chr2:197637096
|
G | A | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.439-3099C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637096 | ||||||
| chr2:197637135
|
G | A | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.439-3138C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637135 | ||||||
| chr2:197637247
|
A | G | 5 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157others(2): Show | 5 | HG02717.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.439-3250T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637247 | ||||||
| chr2:197637271
|
G | T | 2 | a0001c0001t0002g0153a0001c0001t0021g0037 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.439-3274C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637271 | ||||||
| chr2:197637376
|
C | G | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.439-3379G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637376 | ||||||
| chr2:197637529
|
G | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.439-3532C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637529 | ||||||
| chr2:197637551
|
A | T | 2 | a0001c0002t0003g0200a0001c0002t0036g0201 | 2 | NA18962.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.439-3554T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637551 | ||||||
| chr2:197637652
|
G | T | 137 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.439-3655C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637652 | ||||||
| chr2:197637838
|
C | T | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.439-3841G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637838 | ||||||
| chr2:197637914
|
A | G | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.439-3917T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637914 | ||||||
| chr2:197637951
|
T | C | 1 | a0001c0001t0002g0096 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.439-3954A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637951 | ||||||
| chr2:197637989
|
G | A | 1 | a0001c0001t0002g0076 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.439-3992C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637989 | ||||||
| chr2:197637997
|
T | C | 199 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(196): Show | 202 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.439-4000A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197637997 | ||||||
| chr2:197638031
|
C | T | 1 | a0001c0001t0024g0115 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.439-4034G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638031 | ||||||
| chr2:197638045
|
G | A | 1 | a0001c0002t0001g0293 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.439-4048C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638045 | ||||||
| chr2:197638046
|
G | A | 1 | a0001c0001t0003g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.439-4049C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638046 | ||||||
| chr2:197638057
|
A | G | 306 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(303): Show | 309 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.439-4060T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638057 | ||||||
| chr2:197638072
|
G | T | 1 | a0001c0001t0007g0084 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.439-4075C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638072 | ||||||
| chr2:197638118
|
T | C | 56 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(53): Show | 57 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.439-4121A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638118 | ||||||
| chr2:197638159
|
C | G | 56 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(53): Show | 57 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.439-4162G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638159 | ||||||
| chr2:197638165
|
G | C | 1 | a0001c0001t0009g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.439-4168C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638165 | ||||||
| chr2:197638226
|
G | C | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.439-4229C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638226 | ||||||
| chr2:197638253
|
A | G | 80 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(77): Show | 80 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.439-4256T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638253 | ||||||
| chr2:197638256
|
C | T | 83 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(80): Show | 83 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.439-4259G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638256 | ||||||
| chr2:197638295
|
G | C | 1 | a0001c0001t0002g0183 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.439-4298C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638295 | ||||||
| chr2:197638311
|
G | A | 125 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(122): Show | 127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.439-4314C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638311 | ||||||
| chr2:197638326
|
G | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.439-4329C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638326 | ||||||
| chr2:197638439
|
T | A | 1 | a0001c0001t0006g0030 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.439-4442A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638439 | ||||||
| chr2:197638460
|
T | C | 1 | a0001c0001t0006g0030 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.439-4463A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638460 | ||||||
| chr2:197638563
|
C | A | 2 | a0001c0001t0002g0048a0001c0001t0018g0300 | 2 | HG00099.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.439-4566G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638563 | ||||||
| chr2:197638564
|
T | C | 202 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.439-4567A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638564 | ||||||
| chr2:197638568
|
C | T | 1 | a0001c0002t0001g0298 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.439-4571G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638568 | ||||||
| chr2:197638576
|
GT | G | 4 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(1): Show | 6 | HG02559.hp2 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.439-4580delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638576 | ||||||
| chr2:197638627
|
G | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.439-4630C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638627 | ||||||
| chr2:197638784
|
G | C | 1 | a0001c0001t0002g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.439-4787C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638784 | ||||||
| chr2:197638797
|
T | G | 1 | a0001c0002t0004g0260 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.439-4800A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638797 | ||||||
| chr2:197638836
|
G | A | 56 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(53): Show | 57 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.439-4839C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638836 | ||||||
| chr2:197638868
|
C | T | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.439-4871G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638868 | ||||||
| chr2:197638878
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.439-4881G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638878 | ||||||
| chr2:197638881
|
T | G | 1 | a0001c0002t0001g0204 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.439-4884A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638881 | ||||||
| chr2:197638882
|
T | G | 1 | a0001c0002t0001g0204 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.439-4885A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638882 | ||||||
| chr2:197638950
|
G | C | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.439-4953C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638950 | ||||||
| chr2:197638969
|
T | C | 1 | a0001c0001t0004g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.439-4972A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197638969 | ||||||
| chr2:197639099
|
C | T | 2 | a0001c0001t0003g0070a0001c0001t0003g0179 | 2 | HG02145.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.438+5059G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639099 | ||||||
| chr2:197639102
|
G | C | 3 | a0001c0002t0001g0251a0001c0002t0001g0252a0001c0002t0001g0287 | 3 | NA18950.hp2 NA18963.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.438+5056C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639102 | ||||||
| chr2:197639145
|
T | C | 2 | a0001c0002t0001g0194a0001c0002t0001g0195 | 2 | HG00673.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.438+5013A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639145 | ||||||
| chr2:197639235
|
G | A | 1 | a0001c0002t0004g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.438+4923C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639235 | ||||||
| chr2:197639253
|
G | A | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+4905C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639253 | ||||||
| chr2:197639260
|
G | C | 1 | a0003c0004t0002g0131 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.438+4898C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639260 | ||||||
| chr2:197639354
|
C | T | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.438+4804G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639354 | ||||||
| chr2:197639358
|
G | C | 1 | a0001c0001t0003g0020 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.438+4800C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639358 | ||||||
| chr2:197639559
|
C | A | 1 | a0001c0001t0002g0097 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.438+4599G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639559 | ||||||
| chr2:197639559
|
C | T | 2 | a0001c0001t0002g0178a0001c0001t0007g0177 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.438+4599G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639559 | ||||||
| chr2:197639648
|
T | A | 1 | a0001c0001t0003g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.438+4510A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639648 | ||||||
| chr2:197639715
|
C | T | 49 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0166others(46): Show | 50 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.438+4443G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639715 | ||||||
| chr2:197639741
|
G | C | 1 | a0001c0001t0001g0161 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.438+4417C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639741 | ||||||
| chr2:197639754
|
T | C | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.438+4404A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639754 | ||||||
| chr2:197639771
|
T | C | 4 | a0001c0001t0026g0006a0001c0002t0001g0218a0001c0002t0001g0220others(1): Show | 4 | HG03225.hp1 NA18948.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+4387A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639771 | ||||||
| chr2:197639791
|
G | A | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+4367C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639791 | ||||||
| chr2:197639811
|
G | A | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.438+4347C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639811 | ||||||
| chr2:197639812
|
C | T | 1 | a0001c0001t0002g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.438+4346G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639812 | ||||||
| chr2:197639813
|
G | A | 125 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(122): Show | 127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.438+4345C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639813 | ||||||
| chr2:197639820
|
G | T | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.438+4338C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639820 | ||||||
| chr2:197639834
|
A | C | 56 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(53): Show | 57 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.438+4324T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639834 | ||||||
| chr2:197639973
|
A | C | 1 | a0001c0002t0001g0219 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.438+4185T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639973 | ||||||
| chr2:197639999
|
G | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.438+4159C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197639999 | ||||||
| chr2:197640006
|
A | G | 1 | a0001c0002t0003g0261 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.438+4152T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640006 | ||||||
| chr2:197640051
|
A | G | 2 | a0001c0001t0003g0020a0001c0002t0003g0261 | 2 | NA18995.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.438+4107T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640051 | ||||||
| chr2:197640084
|
G | C | 2 | a0001c0001t0003g0069a0001c0002t0003g0261 | 2 | HG02886.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.438+4074C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640084 | ||||||
| chr2:197640093
|
C | G | 56 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(53): Show | 57 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.438+4065G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640093 | ||||||
| chr2:197640094
|
G | A | 1 | a0001c0002t0003g0261 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.438+4064C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640094 | ||||||
| chr2:197640123
|
G | A | 1 | a0001c0002t0003g0261 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.438+4035C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640123 | ||||||
| chr2:197640178
|
A | C | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3980T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640178 | ||||||
| chr2:197640219
|
C | G | 56 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(53): Show | 57 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.438+3939G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640219 | ||||||
| chr2:197640269
|
G | C | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3889C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640269 | ||||||
| chr2:197640278
|
T | C | 6 | a0001c0001t0003g0031a0001c0001t0010g0206a0001c0001t0010g0208others(3): Show | 6 | HG00323.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.438+3880A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640278 | ||||||
| chr2:197640279
|
G | A | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3879C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640279 | ||||||
| chr2:197640299
|
G | C | 7 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0010g0206others(4): Show | 7 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.438+3859C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640299 | ||||||
| chr2:197640330
|
C | T | 1 | a0001c0001t0014g0019 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.438+3828G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640330 | ||||||
| chr2:197640420
|
C | T | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3738G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640420 | ||||||
| chr2:197640421
|
C | G | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3737G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640421 | ||||||
| chr2:197640441
|
G | A | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3717C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640441 | ||||||
| chr2:197640465
|
A | T | 1 | a0001c0002t0001g0255 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.438+3693T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640465 | ||||||
| chr2:197640484
|
A | T | 54 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(51): Show | 55 | HG00323.hp2 HG00408.hp1 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.438+3674T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640484 | ||||||
| chr2:197640489
|
C | G | 127 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.438+3669G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640489 | ||||||
| chr2:197640537
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.438+3621C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640537 | ||||||
| chr2:197640542
|
C | T | 137 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.438+3616G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640542 | ||||||
| chr2:197640543
|
C | T | 1 | a0001c0001t0021g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.438+3615G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640543 | ||||||
| chr2:197640580
|
G | A | 1 | a0001c0002t0001g0254 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.438+3578C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640580 | ||||||
| chr2:197640639
|
C | T | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.438+3519G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640639 | ||||||
| chr2:197640658
|
C | T | 1 | a0001c0001t0012g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.438+3500G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640658 | ||||||
| chr2:197640687
|
CCCGTCTT others(3): Show |
C | 1 | a0001c0001t0010g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.438+3461_438+3470d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640687 | ||||||
| chr2:197640725
|
G | A | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.438+3433C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640725 | ||||||
| chr2:197640744
|
C | T | 80 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(77): Show | 80 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.438+3414G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640744 | ||||||
| chr2:197640869
|
TTTA | T | 3 | a0001c0001t0002g0166a0001c0001t0003g0050a0001c0001t0003g0165 | 3 | HG01069.hp1 HG01515.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.438+3286_438+3288d others(5): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640869 | ||||||
| chr2:197640881
|
C | G | 1 | a0001c0002t0001g0139 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.438+3277G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640881 | ||||||
| chr2:197640940
|
A | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.438+3218T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197640940 | ||||||
| chr2:197641278
|
T | C | 5 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157others(2): Show | 5 | HG02717.hp2 HG02886.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.438+2880A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641278 | ||||||
| chr2:197641742
|
C | T | 49 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0166others(46): Show | 50 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.438+2416G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641742 | ||||||
| chr2:197641758
|
C | T | 13 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(10): Show | 13 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.438+2400G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641758 | ||||||
| chr2:197641807
|
G | A | 1 | a0001c0001t0003g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.438+2351C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641807 | ||||||
| chr2:197641924
|
C | T | 1 | a0001c0001t0007g0084 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.438+2234G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641924 | ||||||
| chr2:197641962
|
C | T | 7 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0008g0063others(4): Show | 7 | HG02922.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.438+2196G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641962 | ||||||
| chr2:197641966
|
A | G | 306 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(303): Show | 309 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.438+2192T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197641966 | ||||||
| chr2:197642416
|
T | C | 6 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(3): Show | 6 | HG02145.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.438+1742A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642416 | ||||||
| chr2:197642535
|
A | G | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.438+1623T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642535 | ||||||
| chr2:197642794
|
G | T | 1 | a0001c0001t0006g0003 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.438+1364C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642794 | ||||||
| chr2:197642923
|
G | A | 1 | a0001c0001t0003g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.438+1235C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642923 | ||||||
| chr2:197642925
|
G | A | 199 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(196): Show | 202 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.438+1233C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642925 | ||||||
| chr2:197642998
|
T | A | 2 | a0001c0001t0003g0033a0001c0001t0003g0034 | 2 | NA18939.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.438+1160A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642998 | ||||||
| chr2:197642998
|
T | C | 1 | a0001c0001t0003g0032 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.438+1160A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197642998 | ||||||
| chr2:197643010
|
C | T | 1 | a0001c0002t0004g0224 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.438+1148G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643010 | ||||||
| chr2:197643067
|
T | G | 3 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0031g0058 | 3 | HG02615.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.438+1091A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643067 | ||||||
| chr2:197643289
|
G | C | 2 | a0001c0001t0017g0146a0001c0001t0017g0147 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.438+869C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643289 | ||||||
| chr2:197643292
|
A | G | 125 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(122): Show | 127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.438+866T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643292 | ||||||
| chr2:197643320
|
T | C | 49 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0166others(46): Show | 50 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.438+838A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643320 | ||||||
| chr2:197643320
|
T | TGGCCTCA others(11): Show |
1 | a0001c0001t0002g0093 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.438+820_438+837dup others(18): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643320 | ||||||
| chr2:197643400
|
G | C | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.438+758C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197643400 | ||||||
| chr2:197644148
|
A | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.438+10T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 3/8 | chr2 | 197644148 | ||||||
| chr2:197644334
|
C | T | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.324-62G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197644334 | ||||||
| chr2:197644476
|
G | A | 1 | a0001c0001t0002g0305 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.324-204C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197644476 | ||||||
| chr2:197644726
|
G | C | 2 | a0001c0002t0003g0200a0001c0002t0036g0201 | 2 | NA18962.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.324-454C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197644726 | ||||||
| chr2:197645041
|
G | T | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.324-769C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197645041 | ||||||
| chr2:197645387
|
C | A | 1 | a0001c0002t0035g0282 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.323+1096G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197645387 | ||||||
| chr2:197645460
|
AG | A | 16 | a0001c0001t0002g0048a0001c0001t0002g0094a0001c0001t0002g0095others(13): Show | 16 | HG00099.hp2 HG00639.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.323+1022delC | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197645460 | ||||||
| chr2:197645516
|
A | G | 1 | a0001c0001t0009g0051 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.323+967T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197645516 | ||||||
| chr2:197645567
|
A | G | 3 | a0001c0001t0003g0057a0001c0001t0003g0071a0001c0001t0013g0072 | 3 | HG02818.hp2 HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.323+916T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197645567 | ||||||
| chr2:197645940
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.323+543G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197645940 | ||||||
| chr2:197646267
|
C | T | 2 | a0001c0001t0017g0146a0001c0001t0017g0147 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.323+216G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197646267 | ||||||
| chr2:197646362
|
G | A | 131 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(128): Show | 133 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.323+121C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197646362 | ||||||
| chr2:197646380
|
C | T | 1 | a0004c0005t0006g0159 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.323+103G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197646380 | ||||||
| chr2:197646420
|
T | A | 1 | a0001c0001t0002g0112 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.323+63A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197646420 | ||||||
| chr2:197646433
|
C | A | 1 | a0001c0001t0002g0112 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.323+50G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197646433 | ||||||
| chr2:197646450
|
C | T | 1 | a0001c0001t0012g0142 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.323+33G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 2/8 | chr2 | 197646450 | ||||||
| chr2:197646886
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.140-220G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197646886 | ||||||
| chr2:197646897
|
C | CA | 198 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.140-232dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197646897 | ||||||
| chr2:197646897
|
C | CAA | 43 | a0001c0001t0002g0096a0001c0001t0002g0097a0001c0001t0002g0113others(40): Show | 44 | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.140-233_140-232dup others(2): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197646897 | ||||||
| chr2:197646908
|
A | AAC | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.140-243_140-242ins others(2): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197646908 | ||||||
| chr2:197646911
|
A | C | 49 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0166others(46): Show | 50 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.140-245T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197646911 | ||||||
| chr2:197647116
|
A | T | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140-450T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197647116 | ||||||
| chr2:197647193
|
A | G | 202 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.140-527T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197647193 | ||||||
| chr2:197647249
|
G | T | 4 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157others(1): Show | 4 | HG02886.hp2 HG03139.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-583C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197647249 | ||||||
| chr2:197647368
|
C | G | 1 | a0001c0001t0021g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.140-702G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197647368 | ||||||
| chr2:197647800
|
A | G | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.140-1134T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197647800 | ||||||
| chr2:197647876
|
AAG | A | 3 | a0001c0002t0001g0262a0001c0002t0001g0263a0001c0002t0002g0264 | 3 | HG01261.hp2 HG02698.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.140-1212_140-1211d others(4): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197647876 | ||||||
| chr2:197648050
|
C | T | 5 | a0001c0001t0008g0063a0001c0001t0011g0059a0001c0001t0011g0060others(2): Show | 5 | HG02976.hp2 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.140-1384G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197648050 | ||||||
| chr2:197648125
|
G | A | 138 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(135): Show | 140 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.140-1459C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197648125 | ||||||
| chr2:197648281
|
A | C | 1 | a0001c0002t0001g0223 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.140-1615T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197648281 | ||||||
| chr2:197648285
|
A | C | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.140-1619T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197648285 | ||||||
| chr2:197649153
|
C | T | 199 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(196): Show | 202 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.140-2487G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649153 | ||||||
| chr2:197649206
|
G | A | 126 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.140-2540C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649206 | ||||||
| chr2:197649283
|
T | C | 1 | a0001c0001t0017g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140-2617A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649283 | ||||||
| chr2:197649750
|
A | G | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140-3084T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649750 | ||||||
| chr2:197649847
|
A | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.140-3181T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649847 | ||||||
| chr2:197649914
|
A | C | 11 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(8): Show | 11 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.140-3248T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649914 | ||||||
| chr2:197649953
|
T | C | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.140-3287A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649953 | ||||||
| chr2:197649964
|
A | G | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.140-3298T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197649964 | ||||||
| chr2:197650121
|
G | A | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.140-3455C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650121 | ||||||
| chr2:197650151
|
G | T | 1 | a0001c0002t0001g0194 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.140-3485C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650151 | ||||||
| chr2:197650200
|
C | T | 131 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(128): Show | 133 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.140-3534G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650200 | ||||||
| chr2:197650526
|
C | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.140-3860G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650526 | ||||||
| chr2:197650530
|
G | A | 4 | a0001c0002t0001g0214a0001c0002t0001g0219a0001c0002t0001g0265others(1): Show | 4 | HG00323.hp1 HG00738.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-3864C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650530 | ||||||
| chr2:197650727
|
A | G | 4 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157others(1): Show | 4 | HG02886.hp2 HG03139.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-4061T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650727 | ||||||
| chr2:197650755
|
G | T | 1 | a0001c0001t0002g0140 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.140-4089C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650755 | ||||||
| chr2:197650812
|
G | A | 126 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.140-4146C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650812 | ||||||
| chr2:197650934
|
T | C | 199 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(196): Show | 202 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.140-4268A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197650934 | ||||||
| chr2:197651134
|
G | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.140-4468C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651134 | ||||||
| chr2:197651176
|
G | A | 199 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(196): Show | 202 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.140-4510C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651176 | ||||||
| chr2:197651285
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | NA18979.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.140-4619A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651285 | ||||||
| chr2:197651345
|
G | A | 2 | a0001c0002t0001g0273a0001c0002t0034g0274 | 2 | HG00639.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.140-4679C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651345 | ||||||
| chr2:197651356
|
C | T | 1 | a0001c0001t0003g0179 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.140-4690G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651356 | ||||||
| chr2:197651361
|
G | A | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-4695C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651361 | ||||||
| chr2:197651544
|
G | A | 1 | a0001c0001t0005g0151 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.140-4878C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651544 | ||||||
| chr2:197651571
|
G | A | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140-4905C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651571 | ||||||
| chr2:197651587
|
G | A | 1 | a0001c0001t0009g0141 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.140-4921C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651587 | ||||||
| chr2:197651592
|
G | A | 2 | a0001c0001t0005g0129a0001c0002t0001g0278 | 2 | NA19068.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.140-4926C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651592 | ||||||
| chr2:197651626
|
A | G | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-4960T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651626 | ||||||
| chr2:197651639
|
C | A | 2 | a0001c0002t0001g0276a0001c0002t0001g0277 | 2 | NA19005.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.140-4973G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197651639 | ||||||
| chr2:197652077
|
C | G | 1 | a0001c0002t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.140-5411G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197652077 | ||||||
| chr2:197652097
|
C | T | 102 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.140-5431G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197652097 | ||||||
| chr2:197652111
|
G | A | 49 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0166others(46): Show | 50 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.140-5445C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197652111 | ||||||
| chr2:197652868
|
A | G | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.140-6202T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197652868 | ||||||
| chr2:197652916
|
A | G | 1 | a0001c0001t0002g0307 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.140-6250T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197652916 | ||||||
| chr2:197653169
|
C | T | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.140-6503G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653169 | ||||||
| chr2:197653182
|
T | G | 1 | a0001c0001t0005g0130 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.140-6516A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653182 | ||||||
| chr2:197653318
|
T | C | 1 | a0001c0001t0003g0035 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.140-6652A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653318 | ||||||
| chr2:197653332
|
A | AC | 308 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(305): Show | 311 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.140-6667dupG | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653332 | ||||||
| chr2:197653338
|
C | T | 57 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0083others(54): Show | 58 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.140-6672G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653338 | ||||||
| chr2:197653612
|
G | A | 1 | a0001c0002t0004g0283 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.140-6946C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653612 | ||||||
| chr2:197653716
|
C | T | 1 | a0001c0001t0002g0132 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.140-7050G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653716 | ||||||
| chr2:197653777
|
T | C | 1 | a0001c0002t0030g0013 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.140-7111A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653777 | ||||||
| chr2:197653985
|
C | G | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.140-7319G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197653985 | ||||||
| chr2:197654061
|
G | A | 1 | a0004c0005t0006g0159 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.140-7395C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654061 | ||||||
| chr2:197654162
|
C | T | 4 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0006g0157others(1): Show | 4 | HG02886.hp2 HG03139.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.140-7496G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654162 | ||||||
| chr2:197654227
|
A | T | 1 | a0001c0001t0003g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.140-7561T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654227 | ||||||
| chr2:197654590
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.140-7924C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654590 | ||||||
| chr2:197654764
|
G | A | 6 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.140-8098C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654764 | ||||||
| chr2:197654864
|
G | A | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-8198C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654864 | ||||||
| chr2:197654904
|
T | C | 202 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.140-8238A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197654904 | ||||||
| chr2:197655179
|
A | G | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.140-8513T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655179 | ||||||
| chr2:197655591
|
C | T | 1 | a0001c0002t0001g0222 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.140-8925G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655591 | ||||||
| chr2:197655658
|
T | C | 1 | a0001c0001t0003g0160 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.140-8992A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655658 | ||||||
| chr2:197655770
|
G | A | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-9104C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655770 | ||||||
| chr2:197655817
|
C | T | 3 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0031g0058 | 3 | HG02615.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-9151G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655817 | ||||||
| chr2:197655831
|
A | C | 54 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(51): Show | 55 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.140-9165T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655831 | ||||||
| chr2:197655891
|
A | G | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.140-9225T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655891 | ||||||
| chr2:197655929
|
A | T | 3 | a0001c0002t0001g0218a0001c0002t0001g0220a0001c0002t0001g0221 | 3 | NA18948.hp1 NA18984.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.140-9263T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655929 | ||||||
| chr2:197655964
|
C | T | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140-9298G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197655964 | ||||||
| chr2:197656068
|
G | A | 1 | a0001c0001t0003g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.140-9402C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656068 | ||||||
| chr2:197656266
|
G | T | 1 | a0001c0001t0002g0307 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.140-9600C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656266 | ||||||
| chr2:197656632
|
T | C | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.140-9966A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656632 | ||||||
| chr2:197656683
|
C | G | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.140-10017G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656683 | ||||||
| chr2:197656766
|
C | T | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.140-10100G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656766 | ||||||
| chr2:197656782
|
G | A | 1 | a0001c0001t0019g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.140-10116C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656782 | ||||||
| chr2:197656833
|
A | G | 1 | a0001c0002t0001g0269 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.140-10167T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656833 | ||||||
| chr2:197656914
|
C | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.140-10248G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197656914 | ||||||
| chr2:197657025
|
TA | T | 125 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(122): Show | 127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.140-10360delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657025 | ||||||
| chr2:197657026
|
A | T | 50 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(47): Show | 51 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.140-10360T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657026 | ||||||
| chr2:197657036
|
A | T | 2 | a0001c0001t0002g0132a0001c0001t0003g0164 | 2 | HG01361.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.140-10370T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657036 | ||||||
| chr2:197657402
|
T | C | 94 | a0001c0002t0001g0009a0001c0002t0001g0139a0001c0002t0001g0189others(91): Show | 94 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.140-10736A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657402 | ||||||
| chr2:197657668
|
TG | T | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.140-11003delC | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657668 | ||||||
| chr2:197657783
|
G | A | 2 | a0001c0001t0002g0043a0001c0001t0002g0099 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.140-11117C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657783 | ||||||
| chr2:197657908
|
A | G | 192 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(189): Show | 195 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.140-11242T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657908 | ||||||
| chr2:197657911
|
C | G | 139 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.140-11245G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197657911 | ||||||
| chr2:197658045
|
T | C | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.140-11379A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658045 | ||||||
| chr2:197658073
|
G | T | 10 | a0001c0001t0002g0042a0001c0001t0002g0049a0001c0001t0002g0081others(7): Show | 10 | HG00735.hp2 HG01258.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.140-11407C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658073 | ||||||
| chr2:197658179
|
AT | A | 195 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(192): Show | 198 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.140-11514delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658179 | ||||||
| chr2:197658182
|
T | A | 2 | a0001c0001t0018g0300a0001c0001t0025g0308 | 2 | HG02015.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.140-11516A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658182 | ||||||
| chr2:197658220
|
G | A | 2 | a0001c0001t0013g0054a0001c0001t0013g0107 | 2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.140-11554C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658220 | ||||||
| chr2:197658284
|
A | T | 1 | a0001c0001t0002g0132 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.140-11618T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658284 | ||||||
| chr2:197658292
|
G | T | 1 | a0001c0001t0007g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.140-11626C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658292 | ||||||
| chr2:197658300
|
A | G | 1 | a0001c0001t0005g0108 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.140-11634T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658300 | ||||||
| chr2:197658331
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.140-11665G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658331 | ||||||
| chr2:197658347
|
C | T | 1 | a0001c0001t0026g0006 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.140-11681G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658347 | ||||||
| chr2:197658449
|
A | G | 2 | a0001c0001t0002g0153a0001c0001t0021g0037 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.140-11783T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658449 | ||||||
| chr2:197658452
|
GT | G | 14 | a0001c0001t0003g0017a0001c0001t0003g0299a0001c0001t0008g0004others(11): Show | 14 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.140-11787delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658452 | ||||||
| chr2:197658452
|
GTT | G | 180 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(177): Show | 183 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.140-11788_140-1178 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658452 | ||||||
| chr2:197658455
|
T | G | 1 | a0003c0004t0002g0131 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.140-11789A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658455 | ||||||
| chr2:197658477
|
G | C | 2 | a0001c0001t0002g0077a0001c0001t0003g0100 | 2 | HG00642.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.140-11811C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658477 | ||||||
| chr2:197658615
|
A | G | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-11949T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658615 | ||||||
| chr2:197658656
|
A | G | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-11990T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658656 | ||||||
| chr2:197658678
|
T | G | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.140-12012A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658678 | ||||||
| chr2:197658817
|
T | C | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.140-12151A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197658817 | ||||||
| chr2:197659016
|
G | T | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140-12350C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659016 | ||||||
| chr2:197659225
|
G | A | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.140-12559C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659225 | ||||||
| chr2:197659301
|
C | A | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-12635G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659301 | ||||||
| chr2:197659381
|
C | T | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.140-12715G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659381 | ||||||
| chr2:197659425
|
C | T | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.140-12759G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659425 | ||||||
| chr2:197659477
|
TA | T | 125 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(122): Show | 127 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.140-12812delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659477 | ||||||
| chr2:197659477
|
TAA | T | 70 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(67): Show | 71 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.140-12813_140-1281 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659477 | ||||||
| chr2:197659478
|
A | T | 1 | a0001c0001t0012g0191 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.140-12812T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659478 | ||||||
| chr2:197659554
|
A | C | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-12888T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659554 | ||||||
| chr2:197659557
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.140-12891G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659557 | ||||||
| chr2:197659584
|
G | T | 2 | a0001c0001t0002g0178a0001c0001t0007g0177 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140-12918C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659584 | ||||||
| chr2:197659586
|
G | C | 2 | a0001c0001t0002g0178a0001c0001t0007g0177 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140-12920C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659586 | ||||||
| chr2:197659587
|
G | T | 2 | a0001c0001t0002g0178a0001c0001t0007g0177 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140-12921C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659587 | ||||||
| chr2:197659589
|
G | A | 2 | a0001c0001t0002g0178a0001c0001t0007g0177 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140-12923C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659589 | ||||||
| chr2:197659590
|
G | A | 2 | a0001c0001t0002g0178a0001c0001t0007g0177 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.140-12924C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659590 | ||||||
| chr2:197659804
|
CA | C | 197 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(194): Show | 200 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.140-13139delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659804 | ||||||
| chr2:197659847
|
A | G | 1 | a0001c0001t0002g0143 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.140-13181T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197659847 | ||||||
| chr2:197660161
|
G | C | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.140-13495C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660161 | ||||||
| chr2:197660297
|
TTA | T | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.140-13633_140-1363 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660297 | ||||||
| chr2:197660313
|
A | C | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-13647T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660313 | ||||||
| chr2:197660360
|
A | G | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.140-13694T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660360 | ||||||
| chr2:197660384
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.140-13718G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660384 | ||||||
| chr2:197660397
|
A | G | 1 | a0001c0002t0004g0275 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.140-13731T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660397 | ||||||
| chr2:197660445
|
G | A | 1 | a0001c0001t0002g0186 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.140-13779C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660445 | ||||||
| chr2:197660587
|
C | CT | 6 | a0001c0001t0002g0183a0001c0001t0004g0144a0001c0001t0004g0145others(3): Show | 6 | HG02615.hp2 HG02922.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.140-13922dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660587 | ||||||
| chr2:197660651
|
G | T | 1 | a0001c0001t0031g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.140-13985C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660651 | ||||||
| chr2:197660755
|
C | T | 3 | a0001c0001t0006g0154a0001c0001t0006g0156a0001c0001t0015g0155 | 3 | HG02886.hp2 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.140-14089G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660755 | ||||||
| chr2:197660854
|
C | T | 1 | a0001c0001t0003g0016 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.140-14188G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197660854 | ||||||
| chr2:197661233
|
AT | A | 193 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(190): Show | 196 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.139+14086delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197661233 | ||||||
| chr2:197661273
|
G | C | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.139+14047C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197661273 | ||||||
| chr2:197661364
|
G | A | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.139+13956C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197661364 | ||||||
| chr2:197661811
|
G | C | 2 | a0001c0002t0001g0267a0001c0002t0001g0268 | 2 | HG01928.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.139+13509C>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197661811 | ||||||
| chr2:197662114
|
C | T | 1 | a0001c0001t0012g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139+13206G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662114 | ||||||
| chr2:197662507
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.139+12813G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662507 | ||||||
| chr2:197662616
|
A | T | 1 | a0001c0001t0003g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.139+12704T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662616 | ||||||
| chr2:197662616
|
AT | A | 8 | a0001c0002t0001g0189a0001c0002t0001g0269a0001c0002t0001g0270others(5): Show | 8 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.139+12703delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662616 | ||||||
| chr2:197662647
|
C | T | 202 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.139+12673G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662647 | ||||||
| chr2:197662743
|
T | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+12577A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662743 | ||||||
| chr2:197662783
|
A | T | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.139+12537T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662783 | ||||||
| chr2:197662827
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.139+12493G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662827 | ||||||
| chr2:197662966
|
A | G | 1 | a0001c0001t0008g0005 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.139+12354T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197662966 | ||||||
| chr2:197663270
|
T | C | 2 | a0001c0002t0004g0284a0001c0002t0004g0285 | 2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.139+12050A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663270 | ||||||
| chr2:197663418
|
G | A | 3 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0031g0058 | 3 | HG02615.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.139+11902C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663418 | ||||||
| chr2:197663443
|
T | C | 1 | a0001c0001t0023g0102 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.139+11877A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663443 | ||||||
| chr2:197663606
|
G | T | 1 | a0001c0001t0019g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139+11714C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663606 | ||||||
| chr2:197663624
|
A | C | 1 | a0001c0001t0003g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.139+11696T>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663624 | ||||||
| chr2:197663691
|
G | A | 3 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0031g0058 | 3 | HG02615.hp2 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.139+11629C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663691 | ||||||
| chr2:197663783
|
T | A | 4 | a0001c0001t0003g0078a0001c0001t0003g0181a0001c0001t0003g0185others(1): Show | 4 | HG02630.hp2 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+11537A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663783 | ||||||
| chr2:197663984
|
T | C | 1 | a0001c0001t0002g0134 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.139+11336A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197663984 | ||||||
| chr2:197664157
|
C | T | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.139+11163G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664157 | ||||||
| chr2:197664275
|
C | T | 126 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.139+11045G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664275 | ||||||
| chr2:197664302
|
G | A | 8 | a0001c0002t0001g0189a0001c0002t0001g0269a0001c0002t0001g0270others(5): Show | 8 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.139+11018C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664302 | ||||||
| chr2:197664446
|
G | A | 2 | a0001c0001t0002g0178a0001c0001t0007g0177 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.139+10874C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664446 | ||||||
| chr2:197664475
|
CA | C | 165 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.139+10844delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664475 | ||||||
| chr2:197664475
|
CAA | C | 29 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0003g0001others(26): Show | 30 | HG00323.hp2 HG01192.hp1 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.139+10843_139+1084 others(6): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664475 | ||||||
| chr2:197664502
|
C | G | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+10818G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664502 | ||||||
| chr2:197664513
|
G | T | 126 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.139+10807C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664513 | ||||||
| chr2:197664586
|
A | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+10734T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664586 | ||||||
| chr2:197664740
|
G | A | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+10580C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664740 | ||||||
| chr2:197664772
|
G | A | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.139+10548C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664772 | ||||||
| chr2:197664825
|
A | T | 1 | a0001c0001t0002g0079 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.139+10495T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664825 | ||||||
| chr2:197664930
|
C | T | 7 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.139+10390G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664930 | ||||||
| chr2:197664931
|
G | A | 1 | a0001c0002t0004g0275 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.139+10389C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197664931 | ||||||
| chr2:197665212
|
G | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+10108C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665212 | ||||||
| chr2:197665224
|
C | A | 5 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0005g0103others(2): Show | 5 | HG00558.hp1 NA18986.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+10096G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665224 | ||||||
| chr2:197665233
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10087G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665233 | ||||||
| chr2:197665234
|
T | A | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10086A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665234 | ||||||
| chr2:197665235
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10085A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665235 | ||||||
| chr2:197665237
|
C | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10083G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665237 | ||||||
| chr2:197665239
|
G | A | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10081C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665239 | ||||||
| chr2:197665241
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10079A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665241 | ||||||
| chr2:197665242
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10078G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665242 | ||||||
| chr2:197665243
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10077T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665243 | ||||||
| chr2:197665248
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10072A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665248 | ||||||
| chr2:197665250
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10070T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665250 | ||||||
| chr2:197665252
|
G | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10068C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665252 | ||||||
| chr2:197665255
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10065T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665255 | ||||||
| chr2:197665256
|
A | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10064T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665256 | ||||||
| chr2:197665258
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10062G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665258 | ||||||
| chr2:197665261
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10059T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665261 | ||||||
| chr2:197665264
|
C | A | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10056G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665264 | ||||||
| chr2:197665267
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10053G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665267 | ||||||
| chr2:197665269
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10051G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665269 | ||||||
| chr2:197665270
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10050T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665270 | ||||||
| chr2:197665272
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10048T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665272 | ||||||
| chr2:197665276
|
A | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10044T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665276 | ||||||
| chr2:197665278
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10042T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665278 | ||||||
| chr2:197665281
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10039G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665281 | ||||||
| chr2:197665283
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10037T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665283 | ||||||
| chr2:197665284
|
T | A | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10036A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665284 | ||||||
| chr2:197665289
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10031A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665289 | ||||||
| chr2:197665293
|
A | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10027T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665293 | ||||||
| chr2:197665294
|
A | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10026T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665294 | ||||||
| chr2:197665296
|
A | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10024T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665296 | ||||||
| chr2:197665299
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10021A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665299 | ||||||
| chr2:197665311
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10009A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665311 | ||||||
| chr2:197665313
|
C | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10007G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665313 | ||||||
| chr2:197665315
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10005A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665315 | ||||||
| chr2:197665316
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10004A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665316 | ||||||
| chr2:197665319
|
T | A | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10001A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665319 | ||||||
| chr2:197665320
|
A | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+10000T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665320 | ||||||
| chr2:197665321
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9999A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665321 | ||||||
| chr2:197665322
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9998A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665322 | ||||||
| chr2:197665323
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9997A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665323 | ||||||
| chr2:197665325
|
C | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9995G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665325 | ||||||
| chr2:197665326
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9994A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665326 | ||||||
| chr2:197665329
|
C | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9991G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665329 | ||||||
| chr2:197665330
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9990A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665330 | ||||||
| chr2:197665331
|
G | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9989C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665331 | ||||||
| chr2:197665373
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9947A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665373 | ||||||
| chr2:197665378
|
T | A | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9942A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665378 | ||||||
| chr2:197665439
|
T | A | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9881A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665439 | ||||||
| chr2:197665440
|
C | G | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9880G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665440 | ||||||
| chr2:197665443
|
G | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+9877C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665443 | ||||||
| chr2:197665508
|
G | A | 5 | a0001c0001t0003g0104a0001c0001t0003g0105a0001c0001t0005g0103others(2): Show | 5 | HG00558.hp1 NA18986.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+9812C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665508 | ||||||
| chr2:197665517
|
C | CTTTTTTT others(3): Show |
38 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0166others(35): Show | 39 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.139+9793_139+9802d others(12): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | ||||||
| chr2:197665517
|
C | CTTTTTTT others(4): Show |
11 | a0001c0001t0002g0153a0001c0001t0003g0010a0001c0001t0003g0016others(8): Show | 11 | HG01243.hp1 HG01516.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.139+9792_139+9802d others(13): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | ||||||
| chr2:197665517
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0021g0037a0001c0001t0031g0058 | 2 | HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.139+9791_139+9802d others(14): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | ||||||
| chr2:197665517
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0006g0156a0001c0001t0006g0157a0001c0001t0025g0308 | 3 | HG02015.hp2 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.139+9790_139+9802d others(15): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | ||||||
| chr2:197665517
|
C | CTTTTTTT others(7): Show |
4 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0006g0154others(1): Show | 4 | HG02886.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.139+9789_139+9802d others(16): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | ||||||
| chr2:197665517
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0002g0307a0001c0001t0005g0187 | 2 | HG01081.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.139+9787_139+9802d others(18): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | ||||||
| chr2:197665517
|
C | CTTTTTTT others(10): Show |
56 | a0001c0001t0001g0125a0001c0001t0002g0042a0001c0001t0002g0043others(53): Show | 57 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.139+9802_139+9803i others(19): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | ||||||
| chr2:197665517
|
C | CTTTTTTT others(11): Show |
53 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0049others(50): Show | 54 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.139+9802_139+9803i others(20): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | ||||||
| chr2:197665517
|
C | CTTTTTTT others(12): Show |
14 | a0001c0001t0002g0075a0001c0001t0002g0076a0001c0001t0002g0077others(11): Show | 14 | HG00642.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.139+9802_139+9803i others(21): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | ||||||
| chr2:197665517
|
C | CTTTTTTT others(13): Show |
8 | a0001c0001t0002g0038a0001c0001t0002g0067a0001c0001t0002g0074others(5): Show | 8 | HG00621.hp2 HG02630.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.139+9802_139+9803i others(22): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | ||||||
| chr2:197665517
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0002g0140a0001c0001t0003g0071 | 2 | HG02896.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.139+9802_139+9803i others(23): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665517 | ||||||
| chr2:197665542
|
C | T | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.139+9778G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665542 | ||||||
| chr2:197665569
|
G | A | 139 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.139+9751C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665569 | ||||||
| chr2:197665631
|
C | T | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.139+9689G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665631 | ||||||
| chr2:197665634
|
C | G | 1 | a0001c0001t0003g0068 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.139+9686G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665634 | ||||||
| chr2:197665776
|
A | ACTGATAT others(2): Show |
55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.139+9535_139+9543d others(11): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665776 | ||||||
| chr2:197665907
|
C | G | 1 | a0001c0002t0001g0215 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.139+9413G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197665907 | ||||||
| chr2:197666205
|
C | A | 3 | a0001c0002t0001g0203a0001c0002t0001g0204a0005c0008t0001g0205 | 3 | HG01255.hp2 NA18981.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.139+9115G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666205 | ||||||
| chr2:197666334
|
C | A | 2 | a0001c0002t0001g0276a0001c0002t0001g0277 | 2 | NA19005.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.139+8986G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666334 | ||||||
| chr2:197666360
|
A | G | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.139+8960T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666360 | ||||||
| chr2:197666507
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.139+8813A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666507 | ||||||
| chr2:197666543
|
A | T | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+8777T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666543 | ||||||
| chr2:197666660
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139+8660G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666660 | ||||||
| chr2:197666700
|
T | C | 1 | a0001c0001t0005g0138 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.139+8620A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666700 | ||||||
| chr2:197666805
|
A | G | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.139+8515T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197666805 | ||||||
| chr2:197667041
|
T | C | 11 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(8): Show | 11 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.139+8279A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197667041 | ||||||
| chr2:197667059
|
G | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+8261C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197667059 | ||||||
| chr2:197667564
|
T | C | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+7756A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197667564 | ||||||
| chr2:197668053
|
A | G | 6 | a0001c0001t0002g0297a0001c0001t0003g0002a0001c0001t0003g0148others(3): Show | 8 | HG01261.hp1 HG01884.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.139+7267T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668053 | ||||||
| chr2:197668270
|
A | T | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+7050T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668270 | ||||||
| chr2:197668302
|
C | T | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+7018G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668302 | ||||||
| chr2:197668340
|
C | T | 1 | a0001c0001t0009g0051 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.139+6980G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668340 | ||||||
| chr2:197668385
|
C | T | 1 | a0001c0001t0005g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.139+6935G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668385 | ||||||
| chr2:197668458
|
A | G | 11 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(8): Show | 11 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.139+6862T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668458 | ||||||
| chr2:197668527
|
C | T | 49 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0166others(46): Show | 50 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.139+6793G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668527 | ||||||
| chr2:197668563
|
C | T | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.139+6757G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668563 | ||||||
| chr2:197668645
|
A | G | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.139+6675T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668645 | ||||||
| chr2:197668882
|
G | T | 139 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(136): Show | 141 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.139+6438C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668882 | ||||||
| chr2:197668950
|
A | G | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+6370T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197668950 | ||||||
| chr2:197669376
|
C | CT | 56 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(53): Show | 57 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.139+5943dupA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669376 | ||||||
| chr2:197669477
|
C | G | 2 | a0001c0001t0017g0146a0001c0001t0017g0147 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.139+5843G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669477 | ||||||
| chr2:197669552
|
C | T | 1 | a0001c0002t0001g0211 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.139+5768G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669552 | ||||||
| chr2:197669591
|
A | G | 1 | a0001c0001t0002g0067 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.139+5729T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669591 | ||||||
| chr2:197669636
|
C | T | 12 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(9): Show | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.139+5684G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669636 | ||||||
| chr2:197669775
|
T | A | 1 | a0001c0002t0001g0278 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.139+5545A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669775 | ||||||
| chr2:197669790
|
C | T | 194 | a0001c0001t0001g0125a0001c0001t0001g0161a0001c0001t0001g0162others(191): Show | 197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.139+5530G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669790 | ||||||
| chr2:197669967
|
C | G | 5 | a0001c0001t0010g0206a0001c0001t0010g0208a0001c0001t0010g0209others(2): Show | 5 | HG02258.hp2 HG02451.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+5353G>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669967 | ||||||
| chr2:197669984
|
G | A | 126 | a0001c0001t0001g0125a0001c0001t0002g0038a0001c0001t0002g0039others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.139+5336C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197669984 | ||||||
| chr2:197670252
|
T | G | 1 | a0001c0001t0019g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139+5068A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670252 | ||||||
| chr2:197670273
|
A | G | 3 | a0001c0002t0001g0203a0001c0002t0001g0204a0005c0008t0001g0205 | 3 | HG01255.hp2 NA18981.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.139+5047T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670273 | ||||||
| chr2:197670384
|
C | T | 2 | a0001c0001t0002g0178a0001c0001t0007g0177 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.139+4936G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670384 | ||||||
| chr2:197670483
|
C | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+4837G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670483 | ||||||
| chr2:197670580
|
CAGG | C | 49 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0166others(46): Show | 50 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.139+4737_139+4739d others(5): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670580 | ||||||
| chr2:197670732
|
TA | T | 60 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(57): Show | 61 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.139+4587delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670732 | ||||||
| chr2:197670830
|
C | T | 1 | a0001c0001t0003g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.139+4490G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670830 | ||||||
| chr2:197670871
|
G | A | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+4449C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670871 | ||||||
| chr2:197670954
|
T | C | 181 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0140others(178): Show | 182 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.139+4366A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670954 | ||||||
| chr2:197670955
|
G | A | 56 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(53): Show | 57 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.139+4365C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197670955 | ||||||
| chr2:197671006
|
A | T | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.139+4314T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671006 | ||||||
| chr2:197671154
|
A | T | 2 | a0001c0002t0003g0200a0001c0002t0036g0201 | 2 | NA18962.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.139+4166T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671154 | ||||||
| chr2:197671423
|
C | T | 4 | a0001c0001t0009g0051a0001c0001t0009g0052a0001c0001t0009g0053others(1): Show | 4 | HG02109.hp1 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.139+3897G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671423 | ||||||
| chr2:197671448
|
C | T | 1 | a0001c0002t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.139+3872G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671448 | ||||||
| chr2:197671615
|
T | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+3705A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671615 | ||||||
| chr2:197671658
|
A | G | 6 | a0001c0002t0001g0195a0001c0002t0001g0287a0001c0002t0002g0196others(3): Show | 6 | HG00673.hp1 HG02015.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.139+3662T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671658 | ||||||
| chr2:197671661
|
A | T | 1 | a0001c0002t0001g0194 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.139+3659T>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671661 | ||||||
| chr2:197671730
|
G | T | 1 | a0001c0001t0021g0037 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.139+3590C>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671730 | ||||||
| chr2:197671855
|
CT | C | 4 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0017g0146others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+3464delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197671855 | ||||||
| chr2:197672175
|
T | A | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+3145A>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197672175 | ||||||
| chr2:197672336
|
T | C | 5 | a0001c0001t0003g0002a0001c0001t0003g0148a0001c0001t0003g0149others(2): Show | 7 | HG01261.hp1 HG02559.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.139+2984A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197672336 | ||||||
| chr2:197672557
|
A | G | 55 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(52): Show | 56 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.139+2763T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197672557 | ||||||
| chr2:197672641
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.139+2679T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197672641 | ||||||
| chr2:197672679
|
T | C | 1 | a0001c0001t0005g0151 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.139+2641A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197672679 | ||||||
| chr2:197672923
|
T | G | 5 | a0001c0002t0004g0281a0001c0002t0004g0283a0001c0002t0004g0284others(2): Show | 5 | HG02055.hp2 HG03491.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.139+2397A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197672923 | ||||||
| chr2:197673049
|
C | T | 1 | a0001c0001t0003g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.139+2271G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197673049 | ||||||
| chr2:197673132
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.139+2188G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197673132 | ||||||
| chr2:197673228
|
C | A | 4 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(1): Show | 4 | HG02717.hp2 HG02896.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+2092G>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197673228 | ||||||
| chr2:197673716
|
G | A | 1 | a0001c0001t0012g0191 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.139+1604C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197673716 | ||||||
| chr2:197673807
|
C | T | 2 | a0001c0001t0002g0048a0001c0001t0018g0300 | 2 | HG00099.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.139+1513G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197673807 | ||||||
| chr2:197673967
|
A | G | 1 | a0001c0001t0003g0015 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.139+1353T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197673967 | ||||||
| chr2:197674063
|
C | T | 4 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0046others(1): Show | 4 | HG02717.hp2 HG02896.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+1257G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674063 | ||||||
| chr2:197674073
|
G | A | 2 | a0001c0001t0008g0007a0001c0001t0008g0008 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.139+1247C>T | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674073 | ||||||
| chr2:197674116
|
A | G | 1 | a0001c0001t0003g0015 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.139+1204T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674116 | ||||||
| chr2:197674339
|
C | CA | 71 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0002g0153others(68): Show | 72 | HG00323.hp2 HG00408.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.139+980dupT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674339 | ||||||
| chr2:197674339
|
C | CAA | 95 | a0001c0001t0002g0193a0001c0001t0002g0202a0001c0001t0002g0279others(92): Show | 95 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.139+979_139+980dup others(2): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674339 | ||||||
| chr2:197674339
|
C | CAAA | 12 | a0001c0002t0001g0287a0001c0002t0001g0290a0001c0002t0001g0293others(9): Show | 12 | HG01928.hp1 HG01978.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.139+978_139+980dup others(3): Show |
RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674339 | ||||||
| chr2:197674339
|
CA | C | 8 | a0001c0001t0002g0038a0001c0001t0002g0039a0001c0001t0002g0040others(5): Show | 8 | HG02015.hp2 HG02970.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.139+980delT | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674339 | ||||||
| chr2:197674359
|
A | G | 1 | a0001c0001t0019g0036 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139+961T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674359 | ||||||
| chr2:197674620
|
T | C | 1 | a0001c0001t0002g0297 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.139+700A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674620 | ||||||
| chr2:197674681
|
A | G | 25 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0015others(22): Show | 26 | HG00323.hp2 HG01192.hp1 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.139+639T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674681 | ||||||
| chr2:197674739
|
T | C | 1 | a0001c0002t0001g0298 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.139+581A>G | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674739 | ||||||
| chr2:197674776
|
C | T | 2 | a0001c0002t0027g0012a0001c0002t0030g0013 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.139+544G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674776 | ||||||
| chr2:197674791
|
CT | C | 8 | a0001c0001t0002g0301a0001c0001t0002g0302a0001c0001t0002g0303others(5): Show | 8 | HG00099.hp1 HG00738.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.139+528delA | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674791 | ||||||
| chr2:197674821
|
A | G | 1 | a0001c0001t0003g0011 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.139+499T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674821 | ||||||
| chr2:197674921
|
C | T | 1 | a0001c0001t0003g0010 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.139+399G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197674921 | ||||||
| chr2:197675130
|
T | G | 1 | a0001c0001t0002g0307 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.139+190A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197675130 | ||||||
| chr2:197675172
|
A | G | 1 | a0001c0002t0001g0009 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.139+148T>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197675172 | ||||||
| chr2:197675242
|
T | G | 1 | a0001c0001t0025g0308 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.139+78A>C | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197675242 | ||||||
| chr2:197675295
|
C | T | 5 | a0001c0001t0008g0004a0001c0001t0008g0005a0001c0001t0008g0007others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+25G>A | RFTN2 | ENSG00000162944.11 | transcript | ENST00000295049.9 | protein_coding | 1/8 | chr2 | 197675295 |